Peptidomimetic macrocycles

ABSTRACT

Provided herein are peptidomimetic macrocycles containing amino acid sequences with at least two modified amino acids that form an intramolecular cross-link that can help to stabilize a secondary structure of the amino acid sequence. Suitable sequences for stabilization include those with homology to the p53 protein. These sequences can bind to the MDM2 and/or MDMX proteins. Also provided herein are methods of using such macrocycles for the treatment of diseases and disorders, such as cancers or other disorders characterized by a low level or low activity of a p53 protein or high level of activity of a MDM2 and/or MDMX protein.

CROSS-REFERENCE

This application claims the benefit of U.S. Provisional Application Nos. 61/599,328, filed Feb. 15, 2012, U.S. Provisional Application No. 61/656,962, filed Jun. 7, 2012, and U.S. Provisional Application No. 61/723,770, filed Nov. 7, 2012; each of which is incorporated herein by reference in their entirety.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Jul. 3, 2014, is named 35224-766.201_SL.txt and is 1,202,046 bytes in size.

BACKGROUND OF THE INVENTION

The human transcription factor protein p53 induces cell cycle arrest and apoptosis in response to DNA damage and cellular stress, and thereby plays a critical role in protecting cells from malignant transformation. The E3 ubiquitin ligase MDM2 (also known as HDM2) negatively regulates p53 function through a direct binding interaction that neutralizes the p53 transactivation activity, leads to export from the nucleus of p53 protein, and targets p53 for degradation via the ubiquitylation-proteasomal pathway. Loss of p53 activity, either by deletion, mutation, or MDM2 overexpression, is the most common defect in human cancers. Tumors that express wild type p53 are vulnerable to pharmacologic agents that stabilize or increase the concentration of active p53. In this context, inhibition of the activities of MDM2 has emerged as a validated approach to restore p53 activity and resensitize cancer cells to apoptosis in vitro and in vivo. MDMX (MDM4) has more recently been identified as a similar negative regulator of p53, and studies have revealed significant structural homology between the p53 binding interfaces of MDM2 and MDMX. The p53-MDM2 and p53-MDMX protein-protein interactions are mediated by the same 15-residue alphα-helical transactivation domain of p53, which inserts into hydrophobic clefts on the surface of MDM2 and MDMX. Three residues within this domain of p53 (F19, W23, and L26) are essential for binding to MDM2 and MDMX.

There remains a considerable need for compounds capable of binding to and modulating the activity of p53, MDM2 and/or MDMX. Provided herein are p53-based peptidomimetic macrocycles that modulate an activity of p53. Also provided herein are p53-based peptidomimetic macrocycles that inhibit the interactions between p53, MDM2 and/or MDMX proteins. Further, provided herein are p53-based peptidomimetic macrocycles that can be used for treating diseases including but not limited to cancer and other hyperproliferative diseases.

SUMMARY OF THE INVENTION

Described herein are stably cross-linked peptides related to a portion of human p53 (“p53 peptidomimetic macrocycles”). These cross-linked peptides contain at least two modified amino acids that together form an intramolecular cross-link that can help to stabilize the alphα-helical secondary structure of a portion of p53 that is thought to be important for binding of p53 to MDM2 and for binding of p53 to MDMX. Accordingly, a cross-linked polypeptide described herein can have improved biological activity relative to a corresponding polypeptide that is not cross-linked. The p53 peptidomimetic macrocycles are thought to interfere with binding of p53 to MDM2 and/or of p53 to MDMX, thereby liberating functional p53 and inhibiting its destruction. The p53 peptidomimetic macrocycles described herein can be used therapeutically, for example to treat cancers and other disorders characterized by an undesirably low level or a low activity of p53, and/or to treat cancers and other disorders characterized by an undesirably high level of activity of MDM2 or MDMX. The p53 peptidomimetic macrocycles can also be useful for treatment of any disorder associated with disrupted regulation of the p53 transcriptional pathway, leading to conditions of excess cell survival and proliferation such as cancer and autoimmunity, in addition to conditions of inappropriate cell cycle arrest and apoptosis such as neurodegeneration and immunedeficiencies. In some embodiments, the p53 peptidomimetic macrocycles bind to MDM2 (e.g., GenBank® Accession No.: 228952; GI:228952) and/or MDMX (also referred to as MDM4; GenBank® Accession No.: 88702791; GI:88702791).

In one aspect, provided herein is a peptidomimetic macrocycle comprising an amino acid sequence which is at least about 60%, 80%, 90%, or 95% identical to an amino acid sequence chosen from the group consisting of the amino acid sequences in Table 1, Table 1a, Table 1b, or Table 1c. Alternatively, an amino acid sequence of said peptidomimetic macrocycle is chosen from the group consisting of the amino acid sequences in Table 4. In some embodiments, the peptidomimetic macrocycle is not a peptide as shown in Table 2a or 2b. In other cases, the peptidomimetic macrocycle does not comprise a structure as shown in Table 2a or 2b. In some embodiments, the peptidomimetic macrocycle has an amino acid sequence chosen from Table 1. In some embodiments, the peptidomimetic macrocycle has an amino acid sequence chosen from Table 1a. In some embodiments, the peptidomimetic macrocycle has an amino acid sequence chosen from Table 1b. In some embodiments, the peptidomimetic macrocycle has an amino acid sequence chosen from Table 1c.

Alternatively, an amino acid sequence of said peptidomimetic macrocycle is chosen as above, and further wherein the macrocycle does not include a thioether or a triazole. In some embodiments, the peptidomimetic macrocycle comprises a helix, such as an α-helix. In other embodiments, the peptidomimetic macrocycle comprises an α,α-disubstituted amino acid. A peptidomimetic macrocycle can comprise a crosslinker linking the α-positions of at least two amino acids. At least one of said two amino acids can be an α,α-disubstituted amino acid.

In some embodiments, provided are peptidomimetic macrocycle of the formula:

wherein:

each A, C, D, and E is independently an amino acid;

B is an amino acid,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-];

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ and L₃ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v and w are independently integers from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10;

u is an integer from 1-10, for example 1-5, 1-3 or 1-2;

x, y and z are independently integers from 0-10, for example the sum of x+y+z is 2, 3, or 6; and

n is an integer from 1-5.

In some embodiments, w>2 and each of the first two amino acid represented by E comprises an uncharged side chain or a negatively charged side chain.

some embodiments, the first C-terminal amino acid and/or the second C-terminal amino acid represented by E comprise a hydrophobic side chain. For example, the first C-terminal amino acid and/or the second C-terminal amino acid represented by E comprises a hydrophobic side chain, for example a large hydrophobic side chain.

In some embodiments, w is between 3 and 1000. For example, the third amino acid represented by E comprises a large hydrophobic side chain.

In other embodiments, the peptidomimetic macrocycle as claimed excludes the sequence of:

-   Ac-RTQATF$r8NQWAibAN1e$TNAibTR-NH₂ (SEQ ID NO: 1),

Ac-RTQATF$r8NQWAibAN1e$TNAibTR-NH₂ (SEQ ID NO: 2),

Ac-$r8SQQTFS$LWRLLAibQN-NH₂ (SEQ ID NO: 3),

Ac-QSQ$r8TFSNLW$LLAibQN-NH₂ (SEQ ID NO: 4),

Ac-QS$r5QTFStNLW$LLAibQN-NH₂ (SEQ ID NO: 5), or

Ac-QSQQ$r8FSNLWR$LAibQN-NH₂ (SEQ ID NO: 6),

In other embodiments, the peptidomimetic macrocycle as claimed excludes the sequence of:

Ac-Q$r8QQTFSN$WRLLAibQN-NH₂ (SEQ ID NO: 7).

Peptidomimetic macrocycles are also provided of the formula:

wherein:

each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8), where each X is an amino acid;

each D and E is independently an amino acid;

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]₁, each being optionally substituted with R₅;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10;

w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10; and

n is an integer from 1-5.

In some embodiments, a peptidomimetic macrocycle has the Formula:

wherein:

each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), where each X is an amino acid;

each D is independently an amino acid;

each E is independently an amino acid, for example an amino acid selected from Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine);

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄-]_(n), each being optionally substituted with R₅;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10;

w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10; and

n is an integer from 1-5.

In some embodiments, a peptidomimetic macrocycle has the Formula:

wherein:

each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least two of Xaa₃, Xaa₅, Xaa₆, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁ (SEQ ID NO: 9), where each X is an amino acid;

each D and E is independently an amino acid;

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-, wherein L comprises at least one double bond in the E configuration;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v is an integer from 1-1000;

w is an integer from 3-1000;

n is an integer from 1-5; and

Xaa₇ is Boc-protected tryptophan.

In some embodiments of any of the Formulas described herein, [D]_(v) is -Leu₁-Thr₂. In other embodiments of the Formulas described herein, each E other than the third amino acid represented by E is an amino acid selected from Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine).

In some embodiments, w is an integer from 3-10, for example 3-6, 3-8, 6-8, or 6-10. In some embodiments, w is 3. In other embodiments, w is 6. In some embodiments, v is an integer from 1-10, for example 2-5. In some embodiments, v is 2.

In some embodiments, peptides disclosed herein bind a binding site defined at least in part by the MDMX amino acid side chains of L17, V46, M50, Y96 (forming the rim of the pocket) and L99. Without being bound by theory, binding to such a binding site improves one or more properties such as binding affinity, induction of apoptosis, in vitro or in vivo anti-tumor efficacy, or reduced ratio of binding affinities to MDMX versus MDM2.

In some embodiments, the peptidomimetic macrocycle has improved binding affinity to MDM2 or MDMX relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In other instances, the peptidomimetic macrocycle has a reduced ratio of binding affinities to MDMX versus MDM2 relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In still other instances, the peptidomimetic macrocycle has improved in vitro anti-tumor efficacy against p53 positive tumor cell lines relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In some embodiments, the peptidomimetic macrocycle shows improved in vitro induction of apoptosis in p53 positive tumor cell lines relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In other instances, the peptidomimetic macrocycle of claim 1, wherein the peptidomimetic macrocycle has an improved in vitro anti-tumor efficacy ratio for p53 positive versus p53 negative or mutant tumor cell lines relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In some instances the improved efficacy ratio in vitro, is 1-29, ≧30-49, or ≧50. In still other instances, the peptidomimetic macrocycle has improved in vivo anti-tumor efficacy against p53 positive tumors relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In some instances the improved efficacy ratio in vivo is −29, ≧30-49, or ≧50. In yet other instances, the peptidomimetic macrocycle has improved in vivo induction of apoptosis in p53 positive tumors relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In some embodiments, the peptidomimetic macrocycle has improved cell permeability relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2. In other cases, the peptidomimetic macrocycle has improved solubility relative to a corresponding peptidomimetic macrocycle where w is 0, 1 or 2.

In some embodiments, Xaa₅ is Glu or an amino acid analog thereof. In some embodiments, Xaa₅ is Glu or an amino acid analog thereof and wherein the peptidomimetic macrocycle has an improved property, such as improved binding affinity, improved solubility, improved cellular efficacy, improved cell permeability, improved in vivo or in vitro anti-tumor efficacy, or improved induction of apoptosis relative to a corresponding peptidomimetic macrocycle where Xaa₅ is Ala.

In some embodiments, the peptidomimetic macrocycle has improved binding affinity to MDM2 or MDMX relative to a corresponding peptidomimetic macrocycle where Xaa₅ is Ala. In other embodiments, the peptidomimetic macrocycle has a reduced ratio of binding affinities to MDMX vs MDM2 relative to a corresponding peptidomimetic macrocycle where Xaa₅ is Ala. In some embodiments, the peptidomimetic macrocycle has improved solubility relative to a corresponding peptidomimetic macrocycle where Xaa₅ is Ala, or the peptidomimetic macrocycle has improved cellular efficacy relative to a corresponding peptidomimetic macrocycle where Xaa₅ is Ala.

In some embodiments, Xaa₅ is Glu or an amino acid analog thereof and wherein the peptidomimetic macrocycle has improved biological activity, such as improved binding affinity, improved solubility, improved cellular efficacy, improved helicity, improved cell permeability, improved in vivo or in vitro anti-tumor efficacy, or improved induction of apoptosis relative to a corresponding peptidomimetic macrocycle where Xaa₅ is Ala.

In some embodiments, the peptidomimetic macrocycle has an activity against a p53+/+ cell line which is at least 2-fold, 3-fold, 5-fold, 10-fold, 20-fold, 30-fold, 50-fold, 70-fold, or 100-fold greater than its binding affinity against a p53−/− cell line. In some embodiments, the peptidomimetic macrocycle has an activity against a p53+/+ cell line which is between 1 and 29-fold, between 30 and 49-fold, or ≧50-fold greater than its binding affinity against a p53−/− cell line. Activity can be measured, for example, as an IC50 value. For example, the p53+/+ cell line is SJSA-1, RKO, HCT-116, or MCF-7 and the p53−/− cell line is RKO-E6 or SW-480. In some embodiments, the peptide has an IC50 against the p53+/+ cell line of less than 1 μM.

In some embodiments, Xaa₅ is Glu or an amino acid analog thereof and the peptidomimetic macrocycle has an activity against a p53+/+ cell line which is at least 10-fold greater than its binding affinity against a p53−/− cell line.

Additionally, a method is provided of treating cancer in a subject comprising administering to the subject a peptidomimetic macrocycle. In some embodiments, the cancer is head and neck cancer, melanoma, lung cancer, breast cancer, or glioma.

Also provided is a method of modulating the activity of p53 or MDM2 or MDMX in a subject comprising administering to the subject a peptidomimetic macrocycle, or a method of antagonizing the interaction between p53 and MDM2 and/or MDMX proteins in a subject comprising administering to the subject such a peptidomimetic macrocycle.

Provided herein is a method of preparing a composition comprising a peptidomimetic macrocycle of Formula (Ia):

comprising an amino acid sequence which is about 60% to about 100% identical to an amino acid sequence selected from the group consisting of the amino acid sequences in Table 1, Table 1a, Table 1b, or Table 1c, the method comprising treating a compound of Formula (II)

with a catalyst to result in the compound of Formula Ia

wherein in the compound(s) of Formulae (Ia) and (II)

each A, C, D, and E is independently an amino acid:

each B is independently an amino acid,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-];

each R₁ and R₂ are independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halogen; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of the D or E amino acids;

each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each L′ is independently a macrocycle-forming linker of the formula -L_(t)-L₂-;

each L₁, L₂ and L₃ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R_(4′)—]_(n), each being optionally substituted with R₅;

each R₄ and R_(4′) is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₇ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

each R₈ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

each v and w are independently integers from 1-1000;

u is an integer from 1-10;

each x, y and z are independently integers from 0-10;

each n is independently an integer from 1-5;

each o is independently an integer from 1 to 15;

each p is independently an integer from 1 to 15;

“(E)” indicates a trans double bond; and

one or more of the amino acids A, C and/or B when B is an amino acid, present in the compounds of Formulae (Ia) and (II), has a side chain bearing a protecting group.

In some embodiments, the protecting group is a nitrogen atom protecting group.

In some embodiments, the protecting group is a Boc group.

In some embodiments, the side chain of the amino acid bearing the protecting group comprises a protected indole.

In some embodiments, the amino acid bearing the protecting group on its side chain is tryptophan (W) that is protected by the protecting group on its indole nitrogen. For example, the protecting group is a Boc group.

In some embodiments, after the step of contacting the compound of Formula II with catalyst the compound of Formula (Ia) is obtained in equal or higher amounts than a corresponding compound which is a Z isomer. For example, after the step of contacting the compound of Formula II with catalyst the compound of Formula (Ia) is obtained in a 2, 3, 4, 5, 6, 7, 8, 9, or 10-fold higher amount than the corresponding compound which is a Z isomer.

In some embodiments, the catalyst is a ruthenium catalyst.

In some embodiments, the method further comprises the step of treating the compounds of Formula (Ia) with a reducing agent or an oxidizing agent.

In some embodiments, the compound of Formula (II) is attached to a solid support. In other embodiments, the compound of Formula (II) is not attached to a solid support.

In some embodiments, the method further comprises removing the protecting group(s) from the compounds of Formula (Ia).

In some embodiments, the ring closing metathesis is conducted at a temperature ranging from about 20° C. to about 80° C.

In some embodiments, the peptidomimetic macrocycle of Formula (Ia) has the Formula:

wherein:

each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least two of Xaa₃, Xaa₅, Xaa₆, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂, (SEQ ID NO: 8), where each X is an amino acid;

each D and E is independently an amino acid;

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-, wherein L comprises at least one double bond in the E configuration;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄-]_(n), each being optionally substituted with R₅;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v is an integer from 1-1000;

w is an integer from 3-1000;

n is an integer from 1-5; and

Xaa₇ is Boc-protected tryptophan.

In some embodiments, the peptidomimetic macrocycle of Formula (Ia) comprises an α-helix.

INCORPORATION BY REFERENCE

All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.

BRIEF DESCRIPTION OF THE DRAWINGS

The novel features of the invention are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present invention will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the invention are utilized, and the accompanying drawings of which:

FIG. 1 shows a structure of peptidomimetic macrocycle 46 (Table 2b), a p53 peptidomimetic macrocycle, complexed with MDMX (Primary SwissProt accession number Q7ZUW7; Entry MDM4_DANRE).

FIG. 2 shows overlaid structures of p53 peptidomimetic macrocycles 142 (Table 2b) and SP43 bound to MDMX (Primary SwissProt accession number Q7ZUW7; Entry MDM4_DANRE).

FIG. 3 shows the effect of SP154, a peptidomimetic macrocycle, on tumor growth in a mouse MCF-7 xenograft model.

FIG. 4 shows the effect of SP249, a peptidomimetic macrocycle, on tumor growth in a mouse MCF-7 xenograft model.

FIG. 5 shows the effect of SP315, a peptidomimetic macrocycle, on tumor growth in a mouse MCF-7 xenograft model.

FIG. 6 shows the effect of SP252, a point mutation of SP154, on tumor growth in a mouse MCF-7 xenograft model.

FIG. 7 shows a plot of solubility for peptidomimetic macrocycles with varying C-terminal extensions.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, the term “macrocycle” refers to a molecule having a chemical structure including a ring or cycle formed by at least 9 covalently bonded atoms.

As used herein, the term “peptidomimetic macrocycle” or “crosslinked polypeptide” refers to a compound comprising a plurality of amino acid residues joined by a plurality of peptide bonds and at least one macrocycle-forming linker which forms a macrocycle between a first naturally-occurring or non-naturally-occurring amino acid residue (or analog) and a second naturally-occurring or non-naturally-occurring amino acid residue (or analog) within the same molecule. Peptidomimetic macrocycle include embodiments where the macrocycle-forming linker connects the α carbon of the first amino acid residue (or analog) to the α carbon of the second amino acid residue (or analog). The peptidomimetic macrocycles optionally include one or more non-peptide bonds between one or more amino acid residues and/or amino acid analog residues, and optionally include one or more non-naturally-occurring amino acid residues or amino acid analog residues in addition to any which form the macrocycle. A “corresponding uncrosslinked polypeptide” when referred to in the context of a peptidomimetic macrocycle is understood to relate to a polypeptide of the same length as the macrocycle and comprising the equivalent natural amino acids of the wild-type sequence corresponding to the macrocycle.

As used herein, the term “stability” refers to the maintenance of a defined secondary structure in solution by a peptidomimetic macrocycle as measured by circular dichroism, NMR or another biophysical measure, or resistance to proteolytic degradation in vitro or in vivo. Non-limiting examples of secondary structures contemplated herein are α-helices, 3₁₀ helices, β-turns, and β-pleated sheets.

As used herein, the term “helical stability” refers to the maintenance of a helical structure by a peptidomimetic macrocycle as measured by circular dichroism or NMR. For example, in some embodiments, a peptidomimetic macrocycle exhibits at least a 1.25, 1.5, 1.75 or 2-fold increase in α-helicity as determined by circular dichroism compared to a corresponding uncrosslinked macrocycle.

The term “amino acid” refers to a molecule containing both an amino group and a carboxyl group. Suitable amino acids include, without limitation, both the D- and L-isomers of the naturally-occurring amino acids, as well as non-naturally occurring amino acids prepared by organic synthesis or other metabolic routes. The term amino acid, as used herein, includes, without limitation, α-amino acids, natural amino acids, non-natural amino acids, and amino acid analogs.

The term “α-amino acid” refers to a molecule containing both an amino group and a carboxyl group bound to a carbon which is designated the α-carbon.

The term “β-amino acid” refers to a molecule containing both an amino group and a carboxyl group in a β configuration.

The term “naturally occurring amino acid” refers to any one of the twenty amino acids commonly found in peptides synthesized in nature, and known by the one letter abbreviations A, R, N, C, D, Q, E, G, H, I, L, K, M, F, P, S, T, W, Y and V.

The following table shows a summary of the properties of natural amino acids:

3- 1- Side- Side-chain Letter Letter chain charge Hydropathy Amino Acid Code Code Polarity (pH 7.4) Index Alanine Ala A nonpolar neutral 1.8 Arginine Arg R polar positive −4.5 Asparagine Asn N polar neutral −3.5 Aspartic acid Asp D polar negative −3.5 Cysteine Cys C polar neutral 2.5 Glutamic acid Glu E polar negative −3.5 Glutamine Gln Q polar neutral −3.5 Glycine Gly G nonpolar neutral −0.4 Histidine His H polar positive(10%) −3.2 neutral(90%) Isoleucine Ile I nonpolar neutral 4.5 Leucine Leu L nonpolar neutral 3.8 Lysine Lys K polar positive −3.9 Methionine Met M nonpolar neutral 1.9 Phenylalanine Phe F nonpolar neutral 2.8 Proline Pro P nonpolar neutral −1.6 Serine Ser S polar neutral −0.8 Threonine Thr T polar neutral −0.7 Tryptophan Trp W nonpolar neutral −0.9 Tyrosine Tyr Y polar neutral −1.3 Valine Val V nonpolar neutral 4.2

“Hydrophobic amino acids” include small hydrophobic amino acids and large hydrophobic amino acids. “Small hydrophobic amino acid” are glycine, alanine, proline, and analogs thereof. “Large hydrophobic amino acids” are valine, leucine, isoleucine, phenylalanine, methionine, tryptophan, and analogs thereof. “Polar amino acids” are serine, threonine, asparagine, glutamine, cysteine, tyrosine, and analogs thereof. “Charged amino acids” are lysine, arginine, histidine, aspartate, glutamate, and analogs thereof.

The term “amino acid analog” refers to a molecule which is structurally similar to an amino acid and which can be substituted for an amino acid in the formation of a peptidomimetic macrocycle. Amino acid analogs include, without limitation, β-amino acids and amino acids where the amino or carboxy group is substituted by a similarly reactive group (e.g., substitution of the primary amine with a secondary or tertiary amine, or substitution of the carboxy group with an ester).

The term “non-natural amino acid” refers to an amino acid which is not one of the twenty amino acids commonly found in peptides synthesized in nature, and known by the one letter abbreviations A, R, N, C, D, Q, E, G, H, I, L, K, M, F, P, S, T, W, Y and V. Non-natural amino acids or amino acid analogs include, without limitation, structures according to the following:

Amino acid analogs include β-amino acid analogs. Examples of β-amino acid analogs include, but are not limited to, the following: cyclic β-amino acid analogs; β-alanine; (R)-β-phenylalanine; (R)-1,2,3,4-tetrahydro-isoquinoline-3-acetic acid; (R)-3-amino-4-(1-naphthyl)-butyric acid; (R)-3-amino-4-(2,4-dichlorophenyl)butyric acid; (R)-3-amino-4-(2-chlorophenyl)-butyric acid; (R)-3-amino-4-(2-cyanophenyl)-butyric acid; (R)-3-amino-4-(2-fluorophenyl)-butyric acid; (R)-3-amino-4-(2-furyl)-butyric acid; (R)-3-amino-4-(2-methylphenyl)-butyric acid; (R)-3-amino-4-(2-naphthyl)-butyric acid; (R)-3-amino-4-(2-thienyl)-butyric acid; (R)-3-amino-4-(2-trifluoromethylphenyl)-butyric acid; (R)-3-amino-4-(3,4-dichlorophenyl)butyric acid; (R)-3-amino-4-(3,4-difluorophenyl)butyric acid; (R)-3-amino-4-(3-benzothienyl)-butyric acid; (R)-3-amino-4-(3-chlorophenyl)-butyric acid; (R)-3-amino-4-(3-cyanophenyl)-butyric acid; (R)-3-amino-4-(3-fluorophenyl)-butyric acid; (R)-3-amino-4-(3-methylphenyl)-butyric acid; (R)-3-amino-4-(3-pyridyl)-butyric acid; (R)-3-amino-4-(3-thienyl)-butyric acid; (R)-3-amino-4-(3-trifluoromethylphenyl)-butyric acid; (R)-3-amino-4-(4-bromophenyl)-butyric acid; (R)-3-amino-4-(4-chlorophenyl)-butyric acid; (R)-3-amino-4-(4-cyanophenyl)-butyric acid; (R)-3-amino-4-(4-fluorophenyl)-butyric acid; (R)-3-amino-4-(4-iodophenyl)-butyric acid; (R)-3-amino-4-(4-methylphenyl)-butyric acid; (R)-3-amino-4-(4-nitrophenyl)-butyric acid; (R)-3-amino-4-(4-pyridyl)-butyric acid; (R)-3-amino-4-(4-trifluoromethylphenyl)-butyric acid; (R)-3-amino-4-pentafluoro-phenylbutyric acid; (R)-3-amino-5-hexenoic acid; (R)-3-amino-5-hexynoic acid; (R)-3-amino-5-phenylpentanoic acid; (R)-3-amino-6-phenyl-5-hexenoic acid; (S)-1,2,3,4-tetrahydro-isoquinoline-3-acetic acid; (S)-3-amino-4-(1-naphthyl)-butyric acid; (S)-3-amino-4-(2,4-dichlorophenyl)butyric acid; (S)-3-amino-4-(2-chlorophenyl)-butyric acid; (S)-3-amino-4-(2-cyanophenyl)-butyric acid; (S)-3-amino-4-(2-fluorophenyl)-butyric acid; (S)-3-amino-4-(2-furyl)-butyric acid; (S)-3-amino-4-(2-methylphenyl)-butyric acid; (S)-3-amino-4-(2-naphthyl)-butyric acid; (S)-3-amino-4-(2-thienyl)-butyric acid; (S)-3-amino-4-(2-trifluoromethylphenyl)-butyric acid; (S)-3-amino-4-(3,4-dichlorophenyl)butyric acid; (S)-3-amino-4-(3,4-difluorophenyl)butyric acid; (S)-3-amino-4-(3-benzothienyl)-butyric acid; (S)-3-amino-4-(3-chlorophenyl)-butyric acid; (S)-3-amino-4-(3-cyanophenyl)-butyric acid; (S)-3-amino-4-(3-fluorophenyl)-butyric acid; (S)-3-amino-4-(3-methylphenyl)-butyric acid; (S)-3-amino-4-(3-pyridyl)-butyric acid; (S)-3-amino-4-(3-thienyl)-butyric acid; (S)-3-amino-4-(3-trifluoromethylphenyl)-butyric acid; (S)-3-amino-4-(4-bromophenyl)-butyric acid; (S)-3-amino-4-(4-chlorophenyl)-butyric acid; (S)-3-amino-4-(4-cyanophenyl)-butyric acid; (S)-3-amino-4-(4-fluorophenyl)-butyric acid; (S)-3-amino-4-(4-iodophenyl)-butyric acid; (S)-3-amino-4-(4-methylphenyl)-butyric acid; (S)-3-amino-4-(4-nitrophenyl)-butyric acid; (S)-3-amino-4-(4-pyridyl)-butyric acid; (S)-3-amino-4-(4-trifluoromethylphenyl)-butyric acid; (S)-3-amino-4-pentafluoro-phenylbutyric acid; (S)-3-amino-5-hexenoic acid; (S)-3-amino-5-hexynoic acid; (S)-3-amino-5-phenylpentanoic acid; (S)-3-amino-6-phenyl-5-hexenoic acid; 1,2,5,6-tetrahydropyridine-3-carboxylic acid; 1,2,5,6-tetrahydropyridine-4-carboxylic acid; 3-amino-3-(2-chlorophenyl)-propionic acid; 3-amino-3-(2-thienyl)-propionic acid; 3-amino-3-(3-bromophenyl)-propionic acid; 3-amino-3-(4-chlorophenyl)-propionic acid; 3-amino-3-(4-methoxyphenyl)-propionic acid; 3-amino-4,4,4-trifluoro-butyric acid; 3-aminoadipic acid; D-β-phenylalanine; β-leucine; L-β-homoalanine; L-β-homoaspartic acid γ-benzyl ester; L-β-homoglutamic acid δ-benzyl ester; L-β-homoisoleucine; L-β-homoleucine; L-β-homomethionine; L-β-homophenylalanine; L-β-homoproline; L-β-homotryptophan; L-β-homovaline; L-Nω-benzyloxycarbonyl-β-homolysine; Nω-L-β-homoarginine; O-benzyl-L-β-homohydroxyproline; O-benzyl-L-β-homoserine; O-benzyl-L-β-homothreonine; O-benzyl-L-β-homotyrosine; γ-trityl-L-β-homoasparagine; (R)-β-phenylalanine; L-β-homoaspartie acid γ-t-butyl ester; L-β-homoglutamic acid δ-t-butyl ester; L-Nω-β-homolysine; Nδ-trityl-L-β-homoglutamine; Nω-2,2,4,6,7-pentamethyl-dihydrobenzofuran-5-sulfonyl-L-β-homoarginine; O-t-butyl-L-β-homohydroxy-proline; O-t-butyl-L-β-homoserine; O-t-butyl-L-β-homothreonine; O-t-butyl-L-β-homotyrosine; 2-aminocyclopentane carboxylic acid; and 2-aminocyclohexane carboxylic acid.

Amino acid analogs include analogs of alanine, valine, glycine or leucine. Examples of amino acid analogs of alanine, valine, glycine, and leucine include, but are not limited to, the following: α-methoxyglycine; α-allyl-L-alanine; α-aminoisobutyric acid; α-methyl-leucine; β-(1-naphthyl)-D-alanine; β-(1-naphthyl)-L-alanine; β-(2-naphthyl)-D-alanine; β-(2-naphthyl)-L-alanine; β-(2-pyridyl)-D-alanine; β-(2-pyridyl)-L-alanine; β-(2-thienyl)-D-alanine; β-(2-thienyl)-L-alanine; β-(3-benzothienyl)-D-alanine; β-(3-benzothienyl)-L-alanine; β-(3-pyridyl)-D-alanine; β-(3-pyridyl)-L-alanine; β-(4-pyridyl)-D-alanine; β-(4-pyridyl)-L-alanine; β-chloro-L-alanine; β-cyano-L-alanin; β-cyclohexyl-D-alanine; β-cyclohexyl-L-alanine; β-cyclopenten-1-yl-alanine; β-cyclopentyl-alanine; β-cyclopropyl-L-Ala-OH.dicyclohexylammonium salt; β-t-butyl-D-alanine; β-t-butyl-L-alanine; γ-aminobutyric acid; L-α,β-diaminopropionic acid; 2,4-dinitro-phenylglycine; 2,5-dihydro-D-phenylglycine; 2-amino-4,4,4-trifluorobutyric acid; 2-fluoro-phenylglycine; 3-amino-4,4,4-trifluoro-butyric acid; 3-fluoro-valine; 4,4,4-trifluoro-valine; 4,5-dehydro-L-leu-OH.dicyclohexylammonium salt; 4-fluoro-D-phenylglycine; 4-fluoro-L-phenylglycine; 4-hydroxy-D-phenylglycine; 5,5,5-trifluoro-leucine; 6-aminohexanoic acid; cyclopentyl-D-Gly-OH.dicyclohexylammonium salt; cyclopentyl-Gly-OH.dicyclohexylammonium salt; D-α,β-diaminopropionic acid; D-α-aminobutyric acid; D-α-t-butylglycine; D-(2-thienyl)glycine; D-(3-thienyl)glycine; D-2-aminocaproic acid; D-2-indanylglycine; D-allylglycine-dicyclohexylammonium salt; D-cyclohexylglycine; D-norvaline; D-phenylglycine; β-aminobutyric acid; β-aminoisobutyric acid; (2-bromophenyl)glycine; (2-methoxyphenyl)glycine; (2-methylphenyl)glycine; (2-thiazoyl)glycine; (2-thienyl)glycine; 2-amino-3-(dimethylamino)-propionic acid; L-1-diaminopropionic acid; L-α-aminobutyric acid; L-α-t-butylglycine; L-(3-thienyl)glycine; L-2-amino-3-(dimethylamino)-propionic acid; L-2-aminocaproic acid dicyclohexyl-ammonium salt; L-2-indanylglycine; L-allylglycine.dicyclohexyl ammonium salt; L-cyclohexylglycine; L-phenylglycine; L-propargylglycine; L-norvaline; N-α-aminomethyl-L-alanine; D-α,γ-diaminobutyric acid; L-α,γ-diaminobutyric acid; β-cyclopropyl-L-alanine; (N-β-(2,4-dinitrophenyl))-L-α,β-diaminopropionic acid; (N-β-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-D—aβ-diaminopropionic acid; (N-β-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-L-α,β-diaminopropionic acid; (N-β-4-methyltrityl)-L-α,β-diaminopropionic acid; (N-β-allyloxycarbonyl)-L-α,β-diaminopropionic acid; (N-γ-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-D-α,γ-diaminobutyric acid; (N-γ-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-L-α,γ-diaminobutyric acid; (N-γ-4-methyltrityl)-D-α,γ-diaminobutyric acid; (N-γ-4-methyltrityl)-L-α,γ-diaminobutyric acid; (N-γ-allyloxycarbonyl)-L-α,γ-diaminobutyric acid; D-α,γ-diaminobutyric acid; 4,5-dehydro-L-leucine; cyclopentyl-D-Gly-OH; cyclopentyl-Gly-OH; D-allylglycine; D-homocyclohexylalanine; L-1-pyrenylalanine; L-2-aminocaproic acid; L-allylglycine; L-homocyclohexylalanine; and N-(2-hydroxy-4-methoxy-Bzl)-Gly-OH.

Amino acid analogs include analogs of arginine or lysine. Examples of amino acid analogs of arginine and lysine include, but are not limited to, the following: citrulline; L-2-amino-3-guanidinopropionic acid; L-2-amino-3-ureidopropionic acid; L-citrulline; Lys(Me)₂-OH; Lys(N₃)—OH; Nδ-benzyloxycarbonyl-L-ornithine; Nω-nitro-D-arginine; Nω-nitro-L-arginine; α-methyl-ornithine; 2,6-diaminoheptanedioic acid; L-ornithine; (Nδ-1-(4,4-dimethyl-2,6-dioxo-cyclohex-1-ylidene)ethyl)-D-ornithine; (Nδ-1-(4,4-dimethyl-2,6-dioxo-cyclohex-1-ylidene)ethyl)-L-ornithine; (Nδ-4-methyltrityl)-D-ornithine; (Nδ-4-methyltrityl)-L-ornithine; D-ornithine; L-ornithine; Arg(Me)(Pbf)-OH; Arg(Me)₂-OH (asymmetrical); Arg(Me)₂-OH (symmetrical); Lys(ivDde)-OH; Lys(Me)2-OH.HCl; Lys(Me3)-OH chloride; Nω-nitro-D-arginine; and Nω-nitro-L-arginine.

Amino acid analogs include analogs of aspartic or glutamic acids. Examples of amino acid analogs of aspartic and glutamic acids include, but are not limited to, the following: α-methyl-D-aspartic acid; α-methyl-glutamic acid; α-methyl-L-aspartic acid; γ-methylene-glutamic acid; (N-γ-ethyl)-L-glutamine; [N-α-(4-aminobenzoyl)]-L-glutamic acid; 2,6-diaminopimelic acid; L-α-aminosuberic acid; D-2-aminoadipic acid; D-α-aminosuberic acid; α-aminopimelic acid; iminodiacetic acid; L-2-aminoadipic acid; threo-β-methyl-aspartic acid; γ-carboxy-D-glutamic acid γ,γ-di-t-butyl ester; γ-carboxy-L-glutamic acid γ,γ-di-t-butyl ester; Glu(OAll)-OH; L-Asu(OtBu)-OH; and pyroglutamic acid.

Amino acid analogs include analogs of cysteine and methionine. Examples of amino acid analogs of cysteine and methionine include, but are not limited to, Cys(farnesyl)-OH, Cys(farnesyl)-OMe, α-methyl-methionine, Cys(2-hydroxyethyl)-OH, Cys(3-aminopropyl)-OH, 2-amino-4-(ethylthio)butyric acid, buthionine, buthioninesulfoximine, ethionine, methionine methylsulfonium chloride, selenomethionine, cysteic acid, [2-(4-pyridyl)ethyl]-DL penicillamine, [2-(4-pyridyl)ethyl]-L-cysteine, 4-methoxybenzyl-D-penicillamine, 4-methoxybenzyl-L-penicillamine, 4-methylbenzyl-D-penicillamine, 4-methylbenzyl-L-penicillamine, benzyl-D-cysteine, benzyl-L-cysteine, benzyl-DL-homocysteine, carbamoyl-L-cysteine, carboxyethyl-L-cysteine, carboxymethyl-L-cysteine, diphenylmethyl-L-cysteine, ethyl-L-cysteine, methyl-L-cysteine, t-butyl-D-cysteine, trityl-L-homocystcinc, trityl-D-penicillamine, cystathioninc, homocystinc, L-homocystinc, (2-aminoethyl)-L-cysteine, seleno-L-cystine, cystathionine, Cys(StBu)-OH, and acetamidomethyl-D-penicillamine.

Amino acid analogs include analogs of phenylalanine and tyrosine. Examples of amino acid analogs of phenylalanine and tyrosine include β-methyl-phenylalanine, β-hydroxyphenylalanine, α-methyl-3-methoxy-DL-phenylalanine, α-methyl-D-phenylalanine, α-methyl-L-phenylalanine, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 2,4-dichloro-phenylalanine, 2-(trifluoromethyl)-D-phenylalanine, 2-(trifluoromethyl)-L-phenylalanine, 2-bromo-D-phenylalanine, 2-bromo-L-phenylalanine, 2-chloro-D-phenylalanine, 2-chloro-L-phenylalanine, 2-cyano-D-phenylalanine, 2-cyano-L-phenylalanine, 2-fluoro-D-phenylalanine, 2-fluoro-L-phenylalanine, 2-methyl-D-phenylalanine, 2-methyl-L-phenylalanine, 2-nitro-D-phenylalanine, 2-nitro-L-phenylalanine, 2;4;5-trihydroxy-phenylalanine, 3,4,5-trifluoro-D-phenylalanine, 3,4,5-trifluoro-L-phenylalanine, 3,4-dichloro-D-phenylalanine, 3,4-dichloro-L-phenylalanine, 3,4-difluoro-D-phenylalanine, 3,4-difluoro-L-phenylalanine, 3,4-dihydroxy-L-phenylalanine, 3,4-dimethoxy-L-phenylalanine, 3,5,3′-triiodo-L-thyronine, 3,5-diiodo-D-tyrosine, 3,5-diiodo-L-tyrosine, 3,5-diiodo-L-thyronine, 3-(trifluoromethyl)-D-phenylalanine, 3-(trifluoromethyl)-L-phenylalanine, 3-amino-L-tyrosine, 3-bromo-D-phenylalanine, 3-bromo-L-phenylalanine, 3-chloro-D-phenylalanine, 3-chloro-L-phenylalanine, 3-chloro-L-tyrosine, 3-cyano-D-phenylalanine, 3-cyano-L-phenylalanine, 3-fluoro-D-phenylalanine, 3-fluoro-L-phenylalanine, 3-fluoro-tyrosine, 3-iodo-D-phenylalanine, 3-iodo-L-phenylalanine, 3-iodo-L-tyrosine, 3-methoxy-L-tyrosine, 3-methyl-D-phenylalanine, 3-methyl-L-phenylalanine, 3-nitro-D-phenylalanine, 3-nitro-L-phenylalanine, 3-nitro-L-tyrosine, 4-(trifluoromethyl)-D-phenylalanine, 4-(trifluoromethyl)-L-phenylalanine, 4-amino-D-phenylalanine, 4-amino-L-phenylalanine, 4-benzoyl-D-phenylalanine, 4-benzoyl-L-phenylalanine, 4-bis(2-chloroethyl)amino-L-phenylalanine, 4-bromo-D-phenylalanine, 4-bromo-L-phenylalanine, 4-chloro-D-phenylalanine, 4-chloro-L-phenylalanine, 4-cyano-D-phenylalanine, 4-cyano-L-phenylalanine, 4-fluoro-D-phenylalanine, 4-fluoro-L-phenylalanine, 4-iodo-D-phenylalanine, 4-iodo-L-phenylalanine, homophenylalanine, thyroxine, 3,3-diphenylalanine, thyronine, ethyl-tyrosine, and methyl-tyrosine.

Amino acid analogs include analogs of proline. Examples of amino acid analogs of proline include, but are not limited to, 3,4-dehydro-proline, 4-fluoro-proline, cis-4-hydroxy-proline, thiazolidine-2-carboxylic acid, and trans-4-fluoro-proline.

Amino acid analogs include analogs of serine and threonine. Examples of amino acid analogs of serine and threonine include, but are not limited to, 3-amino-2-hydroxy-5-methylhexanoic acid, 2-amino-3-hydroxy-4-methylpentanoic acid, 2-amino-3-ethoxybutanoic acid, 2-amino-3-methoxybutanoic acid, 4-amino-3-hydroxy-6-methylheptanoic acid, 2-amino-3-benzyloxypropionic acid, 2-amino-3-benzyloxypropionic acid, 2-amino-3-ethoxypropionic acid, 4-amino-3-hydroxybutanoic acid, and α-methylserine.

Amino acid analogs include analogs of tryptophan. Examples of amino acid analogs of tryptophan include, but are not limited to, the following: α-methyl-tryptophan; β-(3-benzothienyl)-D-alanine; β-(3-benzothienyl)-L-alanine; 1-methyl-tryptophan; 4-methyl-tryptophan; 5-benzyloxy-tryptophan; 5-bromo-tryptophan; 5-chloro-tryptophan; 5-fluoro-tryptophan; 5-hydroxy-tryptophan; 5-hydroxy-L-tryptophan; 5-methoxy-tryptophan; 5-methoxy-L-tryptophan; 5-methyl-tryptophan; 6-bromo-tryptophan; 6-chloro-D-tryptophan; 6-chloro-tryptophan; 6-fluoro-tryptophan; 6-methyl-tryptophan; 7-benzyloxy-tryptophan; 7-bromo-tryptophan; 7-methyl-1-tryptophan; D-1,2,3,4-tetrahydro-norharman-3-carboxylic acid; 6-methoxy-1,2,3,4-tetrahydronorhaman-1-carboxylic acid; 7-azatryptophan; L-1,2,3,4-tetrahydro-norharman-3-carboxylic acid; 5-methoxy-2-methyl-tryptophan; and 6-chloro-L-tryptophan.

In some embodiments, amino acid analogs are racemic. In some embodiments, the D isomer of the amino acid analog is used. In some embodiments, the L isomer of the amino acid analog is used. In other embodiments, the amino acid analog comprises chiral centers that are in the R or S configuration. In still other embodiments, the amino group(s) of a β-amino acid analog is substituted with a protecting group, e.g., tert-butyloxycarbonyl (BOC group), 9-fluorenylmethyloxycarbonyl (FMOC), tosyl, and the like. In yet other embodiments, the carboxylic acid functional group of a β-amino acid analog is protected, e.g., as its ester derivative. In some embodiments the salt of the amino acid analog is used.

A “non-essential” amino acid residue is a residue that can be altered from the wild-type sequence of a polypeptide without abolishing or substantially altering its essential biological or biochemical activity (e.g., receptor binding or activation). An “essential” amino acid residue is a residue that, when altered from the wild-type sequence of the polypeptide, results in abolishing or substantially abolishing the polypeptide's essential biological or biochemical activity.

A “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., K, R, H), acidic side chains (e.g., D, E), uncharged polar side chains (e.g., G, N, Q, S, T, Y, C), nonpolar side chains (e.g., A, V, L, T, P, F, M, W), beta-branched side chains (e.g., T, V, I) and aromatic side chains (e.g., Y, F, W, H). Thus, a predicted nonessential amino acid residue in a polypeptide, for example, is replaced with another amino acid residue from the same side chain family. Other examples of acceptable substitutions are substitutions based on isosteric considerations (e.g. norleucine for methionine) or other properties (e.g. 2-thienylalanine for phenylalanine, or 6-Cl-tryptophan for tryptophan).

The term “capping group” refers to the chemical moiety occurring at either the carboxy or amino terminus of the polypeptide chain of the subject peptidomimetic macrocycle. The capping group of a carboxy terminus includes an unmodified carboxylic acid (i.e. —COOH) or a carboxylic acid with a substituent. For example, the carboxy terminus can be substituted with an amino group to yield a carboxamide at the C-terminus. Various substituents include but are not limited to primary and secondary amines, including pegylated secondary amines. Representative secondary amine capping groups for the C-terminus include:

The capping group of an amino terminus includes an unmodified amine (i.e. —NH₂) or an amine with a substituent. For example, the amino terminus can be substituted with an acyl group to yield a carboxamide at the N-terminus Various substituents include but are not limited to substituted acyl groups, including C₁-C₆ carbonyls, C₇-C₃₀ carbonyls, and pegylated carbamates. Representative capping groups for the N-terminus include, but are not limited to, 4-FBzl (4-fluoro-benzyl) and the following:

The term “member” as used herein in conjunction with macrocycles or macrocycle-forming linkers refers to the atoms that form or can form the macrocycle, and excludes substituent or side chain atoms. By analogy, cyclodecane, 1,2-difluoro-decane and 1,3-dimethyl cyclodecane are all considered ten-membered macrocycles as the hydrogen or fluoro substituents or methyl side chains do not participate in forming the macrocycle.

The symbol “

” when used as part of a molecular structure refers to a single bond or a trans or cis double bond.

The term “amino acid side chain” refers to a moiety attached to the α-carbon (or another backbone atom) in an amino acid. For example, the amino acid side chain for alanine is methyl, the amino acid side chain for phenylalanine is phenylmethyl, the amino acid side chain for cysteine is thiomethyl, the amino acid side chain for aspartate is carboxymethyl, the amino acid side chain for tyrosine is 4-hydroxyphenylmethyl, etc. Other non-naturally occurring amino acid side chains are also included, for example, those that occur in nature (e.g., an amino acid metabolite) or those that are made synthetically (e.g., an α,α di-substituted amino acid).

The term “α,α di-substituted amino” acid refers to a molecule or moiety containing both an amino group and a carboxyl group bound to a carbon (the α-carbon) that is attached to two natural or non-natural amino acid side chains.

The term “polypeptide” encompasses two or more naturally or non-naturally-occurring amino acids joined by a covalent bond (e.g., an amide bond). Polypeptides as described herein include full length proteins (e.g., fully processed proteins) as well as shorter amino acid sequences (e.g., fragments of naturally-occurring proteins or synthetic polypeptide fragments).

The term “first C-terminal amino acid” refers to the amino acid which is closest to the C-terminus. The term “second C-terminal amino acid” refers to the amino acid attached at the N-terminus of the first C-terminal amino acid.

The term “macrocyclization reagent” or “macrocycle-forming reagent” as used herein refers to any reagent which can be used to prepare a peptidomimetic macrocycle by mediating the reaction between two reactive groups. Reactive groups can be, for example, an azide and alkyne, in which case macrocyclization reagents include, without limitation, Cu reagents such as reagents which provide a reactive Cu(I) species, such as CuBr, CuI or CuOTf, as well as Cu(II) salts such as Cu(CO₂CH₃)₂, CuSO₄, and CuCl₂ that can be converted in situ to an active Cu(I) reagent by the addition of a reducing agent such as ascorbic acid or sodium ascorbate. Macrocyclization reagents can additionally include, for example, Ru reagents known in the art such as Cp*RuCl(PPh₃)₂, [Cp*RuCl]₄ or other Ru reagents which can provide a reactive Ru(II) species. In other cases, the reactive groups are terminal olefins. In such embodiments, the macrocyclization reagents or macrocycle-forming reagents are metathesis catalysts including, but not limited to, stabilized, late transition metal carbene complex catalysts such as Group VIII transition metal carbene catalysts. For example, such catalysts are Ru and Os metal centers having a +2 oxidation state, an electron count of 16 and pentacoordinated. In other examples, catalysts have W or Mo centers. Various catalysts are disclosed in Grubbs et al., “Ring Closing Metathesis and Related Processes in Organic Synthesis” Acc. Chem. Res. 1995, 28, 446-452, U.S. Pat. No. 5,811,515; U.S. Pat. No. 7,932,397; U.S. Application No. 2011/0065915; U.S. Application No. 2011/0245477; Yu et al., “Synthesis of Macrocyclic Natural Products by Catalyst-Controlled Stereoselective Ring-Closing Metathesis,” Nature 2011, 479, 88; and Peryshkov et al., “Z-Selective Olefin Metathesis Reactions Promoted by Tungsten Oxo Alkylidene Complexes,” J. Am. Chem. Soc. 2011, 133, 20754. In yet other cases, the reactive groups are thiol groups. In such embodiments, the macrocyclization reagent is, for example, a linker functionalized with two thiol-reactive groups such as halogen groups.

The term “halo” or “halogen” refers to fluorine, chlorine, bromine or iodine or a radical thereof.

The term “alkyl” refers to a hydrocarbon chain that is a straight chain or branched chain, containing the indicated number of carbon atoms. For example, C₁-C₁₀ indicates that the group has from 1 to 10 (inclusive) carbon atoms in it. In the absence of any numerical designation, “alkyl” is a chain (straight or branched) having 1 to 20 (inclusive) carbon atoms in it.

The term “alkylene” refers to a divalent alkyl (i.e., —R—).

The term “alkenyl” refers to a hydrocarbon chain that is a straight chain or branched chain having one or more carbon-carbon double bonds. The alkenyl moiety contains the indicated number of carbon atoms. For example, C₂-C₁₀ indicates that the group has from 2 to 10 (inclusive) carbon atoms in it. The term “lower alkenyl” refers to a C₂-C₆ alkenyl chain. In the absence of any numerical designation, “alkenyl” is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.

The term “alkynyl” refers to a hydrocarbon chain that is a straight chain or branched chain having one or more carbon-carbon triple bonds. The alkynyl moiety contains the indicated number of carbon atoms. For example, C₂-C₁₀ indicates that the group has from 2 to 10 (inclusive) carbon atoms in it. The term “lower alkynyl” refers to a C₂-C₆ alkynyl chain. In the absence of any numerical designation, “alkynyl” is a chain (straight or branched) having 2 to 20 (inclusive) carbon atoms in it.

The term “aryl” refers to a 6-carbon monocyclic or 10-carbon bicyclic aromatic ring system wherein 0, 1, 2, 3, or 4 atoms of each ring are substituted by a substituent. Examples of aryl groups include phenyl, naphthyl and the like. The term “arylalkoxy” refers to an alkoxy substituted with aryl.

“Arylalkyl” refers to an aryl group, as defined above, wherein one of the aryl group's hydrogen atoms has been replaced with a C₁-C₅ alkyl group, as defined above. Representative examples of an arylalkyl group include, but are not limited to, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2-ethylphenyl, 3-ethylphenyl, 4-ethylphenyl, 2-propylphenyl, 3-propylphenyl, 4-propylphenyl, 2-butylphenyl, 3-butylphenyl, 4-butylphenyl, 2-pentylphenyl, 3-pentylphenyl, 4-pentylphenyl, 2-isopropylphenyl, 3-isopropylphenyl, 4-isopropylphenyl, 2-isobutylphenyl, isobutylphenyl, 4-isobutylphenyl, 2-sec-butylphenyl, 3-sec-butylphenyl, 4-sec-butylphenyl, butylphenyl, 3-t-butylphenyl and 4-t-butylphenyl.

“Arylamido” refers to an aryl group, as defined above, wherein one of the aryl group's hydrogen atoms has been replaced with one or more —C(O)NH₂ groups. Representative examples of an arylamido group include 2-C(O)NH2-phenyl, 3-C(O)NH₂-phenyl, 4-C(O)NH₂-phenyl, 2-C(O)NH₂-pyridyl, 3-C(O)NH₂-pyridyl, and 4-C(O)NH₂-pyridyl,

“Alkylheterocycle” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a heterocycle. Representative examples of an alkylheterocycle group include, but are not limited to, —CH₂CH₂-morpholine, —CH₂CH₂-piperidine, —CH₂CH₂CH₂-morpholine, and —CH₂CH₂CH₂-imidazole.

“Alkylamido” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a —C(O)NH₂ group. Representative examples of an alkylamido group include, but are not limited to, —CH₂—C(O)NH₂, —CH₂CH₂—C(O)NH₂, —CH₂CH₂CH₂C(O)NH₂, —CH₂CH₂CH₂CH₂C(O)NH₂, —CH₂CH₂CH₂CH₂CH₂C(O)NH₂, —CH₂CH(C(O)NH₂)CH₃, —CH₂CH(C(O)NH₂)CH₂CH₃, —CH(C(O)NH₂)CH₂CH₃, —C(CH₃)₂CH₂C(O)NH₂, —CH₂—CH₂—NH—C(O)—CH₃, —CH₂—CH₂—NH—C(O)—CH₃—CH₃, and —CH₂—CH₂—NH—C(O)—CH═CH₂.

“Alkanol” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a hydroxyl group. Representative examples of an alkanol group include, but are not limited to, —CH₂OH, —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH₂CH₂CH₂OH, —CH₂CH₂CH₂ CH₂CH₂OH, —CH₂CH(OH)CH₃, —CH₂CH(OH)CH₂CH₃, —CH(OH)CH₃ and —C(CH₃)₂CH₂OH.

“Alkylcarboxy” refers to a C₁-C₅ alkyl group, as defined above, wherein one of the C₁-C₅ alkyl group's hydrogen atoms has been replaced with a —COOH group. Representative examples of an alkylcarboxy group include, but are not limited to, —CH₂COOH, —CH₂CH₂COOH, —CH₂CH₂CH₂COOH, —CH₂CH₂CH₂CH₂COOH, —CH₂CH(COOH)CH₃, —CH₂CH₂CH₂CH₂CH₂COOH, —CH₂CH(COOH)CH₂CH₃, —CH(COOH)CH₂CH₃ and —C(CH₃)₂CH₂COOH.

The term “cycloalkyl” as employed herein includes saturated and partially unsaturated cyclic hydrocarbon groups having 3 to 12 carbons, preferably 3 to 8 carbons, and more preferably 3 to 6 carbons, wherein the cycloalkyl group additionally is optionally substituted. Some cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.

The term “heteroaryl” refers to an aromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of O, N, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2, 3, or 4 atoms of each ring are substituted by a substituent. Examples of heteroaryl groups include pyridyl, furyl or furanyl, imidazolyl, benzimidazolyl, pyrimidinyl, thiophenyl or thienyl, quinolinyl, indolyl, thiazolyl, and the like.

The term “heteroarylalkyl” or the term “heteroaralkyl” refers to an alkyl substituted with a heteroaryl. The term “heteroarylalkoxy” refers to an alkoxy substituted with heteroaryl.

The term “heteroarylalkyl” or the term “heteroaralkyl” refers to an alkyl substituted with a heteroaryl. The term “heteroarylalkoxy” refers to an alkoxy substituted with heteroaryl.

The term “heterocyclyl” refers to a nonaromatic 5-8 membered monocyclic, 8-12 membered bicyclic, or 11-14 membered tricyclic ring system having 1-3 heteroatoms if monocyclic, 1-6 heteroatoms if bicyclic, or 1-9 heteroatoms if tricyclic, said heteroatoms selected from O, N, or S (e.g., carbon atoms and 1-3, 1-6, or 1-9 heteroatoms of O, N, or S if monocyclic, bicyclic, or tricyclic, respectively), wherein 0, 1, 2 or 3 atoms of each ring are substituted by a substituent. Examples of heterocyclyl groups include piperazinyl, pyrrolidinyl, dioxanyl, morpholinyl, tetrahydrofuranyl, and the like.

The term “substituent” refers to a group replacing a second atom or group such as a hydrogen atom on any molecule, compound or moiety. Suitable substituents include, without limitation, halo, hydroxy, mercapto, oxo, nitro, haloalkyl, alkyl, alkaryl, aryl, aralkyl, alkoxy, thioalkoxy, aryloxy, amino, alkoxycarbonyl, amido, carboxy, alkanesulfonyl, alkylcarbonyl, and cyano groups.

In some embodiments, the compounds disclosed herein contain one or more asymmetric centers and thus occur as racemates and racemic mixtures, single enantiomers, individual diastereomers and diastereomeric mixtures. All such isomeric forms of these compounds are included unless expressly provided otherwise. In some embodiments, the compounds disclosed herein are also represented in multiple tautomeric forms, in such instances, the compounds include all tautomeric forms of the compounds described herein (e.g., if alkylation of a ring system results in alkylation at multiple sites, the invention includes all such reaction products). All such isomeric forms of such compounds are included unless expressly provided otherwise. All crystal forms of the compounds described herein are included unless expressly provided otherwise.

As used herein, the terms “increase” and “decrease” mean, respectively, to cause a statistically significantly (i.e., p<0.1) increase or decrease of at least 5%.

As used herein, the recitation of a numerical range for a variable is intended to convey that the variable is equal to any of the values within that range. Thus, for a variable which is inherently discrete, the variable is equal to any integer value within the numerical range, including the end-points of the range. Similarly, for a variable which is inherently continuous, the variable is equal to any real value within the numerical range, including the end-points of the range. As an example, and without limitation, a variable which is described as having values between 0 and 2 takes the values 0, 1 or 2 if the variable is inherently discrete, and takes the values 0.0, 0.1, 0.01, 0.001, or any other real values >0 and <2 if the variable is inherently continuous.

As used herein, unless specifically indicated otherwise, the word “or” is used in the inclusive sense of “and/or” and not the exclusive sense of “either/or.”

The term “on average” represents the mean value derived from performing at least three independent replicates for each data point.

The term “biological activity” encompasses structural and functional properties of a macrocycle. Biological activity is, for example, structural stability, alpha-hclicity, affinity for a target, resistance to proteolytic degradation, cell penetrability, intracellular stability, in vivo stability, or any combination thereof.

The term “binding affinity” refers to the strength of a binding interaction, for example between a peptidomimetic macrocycle and a target. Binding affinity can be expressed, for example, as an equilibrium dissociation constant (“K_(D)”), which is expressed in units which are a measure of concentration (e.g. M, mM, μM, nM etc). Numerically, binding affinity and K_(D) values vary inversely, such that a lower binding affinity corresponds to a higher K_(D) value, while a higher binding affinity corresponds to a lower K_(D) value. Where high binding affinity is desirable, “improved” binding affinity refers to higher binding affinity and therefore lower K_(D) values.

The term “in vitro efficacy” refers to the extent to which a test compound, such as a peptidomimetic macrocycle, produces a beneficial result in an in vitro test system or assay. In vitro efficacy can be measured, for example, as an “IC₅₀” or “EC₅₀” value, which represents the concentration of the test compound which produces 50% of the maximal effect in the test system. The term “ratio of in vitro efficacies” or “in vitro efficacy ratio” refers to the ratio of IC₅₀ or EC₅₀ values from a first assay (the numerator) versus a second assay (the denominator). Consequently, an improved in vitro efficacy ratio for Assay 1 versus Assay 2 refers to a lower value for the ratio expressed as IC₅₀(Assay 1)/IC₅₀(Assay 2) or alternatively as EC₅₀(Assay 1)/EC₅₀(Assay 2). This concept can also be characterized as “improved selectivity” in Assay 1 versus Assay 2, which can be due either to a decrease in the IC₅₀ or EC₅₀ value for Target 1 or an increase in the value for the IC₅₀ or EC₅₀ value for Target 2.

The details of one or more particular embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.

Peptidomimetic Macrocycles

In some embodiments, a peptidomimetic macrocycle has the Formula (I):

wherein:

each A, C, D, and E is independently an amino acid (including natural or non-natural amino acids, and amino acid analogs) and the terminal D and E independently optionally include a capping group;

B is an amino acid (including natural or non-natural amino acids, and amino acid analogs),

[—NH-L₃-CO-], [—NH-L₃-SO₂—], or [—NH-L₃-];

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

L is a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v and w are independently integers from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10;

u is an integer from 1-10, for example 1-5, 1-3 or 1-2;

x, y and z are independently integers from 0-10, for example the sum of x+y+z is 2, 3, or 6; and

n is an integer from 1-5.

In some embodiments, v and w are integers between 1-30. In some embodiments, w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10. In some embodiments, the sum of x+y+z is 3 or 6. In some embodiments, the sum of x+y+z is 3. In other embodiments, the sum of x+y+z is 6.

In some embodiments, peptidomimetic macrocycles are also provided of the formula:

wherein:

each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8), where each X is an amino acid;

each D and E is independently an amino acid;

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20 or 1-10;

w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10; and

n is an integer from 1-5.

In some embodiments, v and w are integers between 1-30. In some embodiments, w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10. In some embodiments, the sum of x+y+z is 3 or 6. In some embodiments, the sum of x+y+z is 3. In other embodiments, the sum of x+y+z is 6.

In some embodiments of any of the Formulas described herein, at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least four of Xaa₃, Xaa, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least five of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least six of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8). In other embodiments, at least seven of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8).

In some embodiments, a peptidomimetic macrocycle has the Formula:

wherein:

each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is individually an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), where each X is an amino acid;

each D is independently an amino acid;

each E is independently an amino acid, for example an amino acid selected from Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine);

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstitutcd or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

each L or L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue;

R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue;

v is an integer from 1-1000, for example 1-500, 1-200, 1-100, 1-50, 1-30, 1-20, or 1-10;

w is an integer from 3-1000, for example 3-500, 3-200, 3-100, 3-50, 3-30, 3-20, or 3-10; and

n is an integer from 1-5.

In some embodiments of the above Formula, at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9). In other embodiments of the above Formula, at least four of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₅, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9). In other embodiments of the above Formula, at least five of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9). In other embodiments of the above Formula, at least six of Xaa₈, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9). In other embodiments of the above Formula, at least seven of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₅, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala_(t2) (SEQ ID NO: 9)

In some embodiments, w is an integer from 3-10, for example 3-6, 3-8, 6-8, or 6-10. In some embodiments, w is 3. In other embodiments, w is 6. In some embodiments, v is an integer from 1-10, for example 2-5. In some embodiments, v is 2.

In an embodiment of any of the Formulas described herein, L₁ and L₂, either alone or in combination, do not form a triazole or a thioether.

In one example, at least one of R₁ and R₂ is alkyl, unsubstituted or substituted with halo-. In another example, both R₁ and R₂ are independently alkyl, unsubstituted or substituted with halo-. In some embodiments, at least one of R₁ and R₂ is methyl. In other embodiments, R₁ and R₂ are methyl.

In some embodiments, x+y+z is at least 3. In other embodiments, x+y+z is 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10. In some embodiments, the sum of x+y+z is 3 or 6. In some embodiments, the sum of x+y+z is 3. In other embodiments, the sum of x+y+z is 6. Each occurrence of A, B, C, D or E in a macrocycle or macrocycle precursor is independently selected. For example, a sequence represented by the formula [A]_(x), when x is 3, encompasses embodiments where the amino acids are not identical, e.g. Gln-Asp-Ala as well as embodiments where the amino acids are identical, e.g. Gln-Gln-Gln. This applies for any value of x, y, or z in the indicated ranges. Similarly, when u is greater than 1, each compound can encompass peptidomimetic macrocycles which are the same or different. For example, a compound can comprise peptidomimetic macrocycles comprising different linker lengths or chemical compositions.

In some embodiments, the peptidomimetic macrocycle comprises a secondary structure which is an α-helix and R₈ is —H, allowing intrahelical hydrogen bonding. In some embodiments, at least one of A, B, C, D or E is an α,α-disubstituted amino acid. In one example, B is an α,α-disubstituted amino acid. For instance, at least one of A, B, C, D or E is 2-aminoisobutyric acid. In other embodiments, at least one of A, B, C, D or E is

In other embodiments, the length of the macrocycle-forming linker L as measured from a first Cα to a second Cα is selected to stabilize a desired secondary peptide structure, such as an α-helix formed by residues of the peptidomimetic macrocycle including, but not necessarily limited to, those between the first Cα to a second Cα.

In one embodiment, the peptidomimetic macrocycle of Formula (I) is:

wherein each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-.

In related embodiments, the peptidomimetic macrocycle of Formula (I) is:

wherein each R₁′ and R₂′ is independently an amino acid.

In other embodiments, the peptidomimetic macrocycle of Formula (I) is a compound of any of the formulas shown below:

wherein “AA” represents any natural or non-natural amino acid side chain and

is [D]_(v), [E]_(w) as defined above, and n is an integer between 0 and 20, 50, 100, 200, 300, 400 or 500. In some embodiments, n is 0. In other embodiments, n is less than 50.

Exemplary embodiments of the macrocycle-forming linker L are shown below.

In other embodiments, D and/or E in the compound of Formula I are further modified in order to facilitate cellular uptake. In some embodiments, lipidating or PEGylating a peptidomimetic macrocycle facilitates cellular uptake, increases bioavailability, increases blood circulation, alters pharmacokinetics, decreases immunogenicity and/or decreases the needed frequency of administration.

In other embodiments, at least one of [D] and [E] in the compound of Formula I represents a moiety comprising an additional macrocycle-forming linker such that the peptidomimetic macrocycle comprises at least two macrocycle-forming linkers. In a specific embodiment, a peptidomimetic macrocycle comprises two macrocycle-forming linkers. In an embodiment, u is 2.

In some embodiments, any of the macrocycle-forming linkers described herein can be used in any combination with any of the sequences shown in Table 1, Table 1a, Table 1b, or Table 1c and also with any of the R-substituents indicated herein.

In some embodiments, the peptidomimetic macrocycle comprises at least one α-helix motif. For example, A, B and/or C in the compound of Formula I include one or more a-helices. As a general matter, a-helices include between 3 and 4 amino acid residues per turn. In some embodiments, the α-helix of the peptidomimetic macrocycle includes 1 to 5 turns and, therefore, 3 to 20 amino acid residues. In specific embodiments, the α-helix includes 1 turn, 2 turns, 3 turns, 4 turns, or 5 turns. In some embodiments, the macrocycle-forming linker stabilizes an α-helix motif included within the peptidomimetic macrocycle. Thus, in some embodiments, the length of the macrocycle-forming linker L from a first Cα to a second Cα is selected to increase the stability of an α-helix. In some embodiments, the macrocycle-forming linker spans from 1 turn to 5 turns of the α-helix. In some embodiments, the macrocycle-forming linker spans approximately 1 turn, 2 turns, 3 turns, 4 turns, or 5 turns of the α-helix. In some embodiments, the length of the macrocycle-forming linker is approximately 5 Å to 9 Å per turn of the α-helix, or approximately 6 Å to 8 Å per turn of the α-helix. Where the macrocycle-forming linker spans approximately 1 turn of an α-helix, the length is equal to approximately 5 carbon-carbon bonds to 13 carbon-carbon bonds, approximately 7 carbon-carbon bonds to 11 carbon-carbon bonds, or approximately 9 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 2 turns of an α-helix, the length is equal to approximately 8 carbon-carbon bonds to 16 carbon-carbon bonds, approximately 10 carbon-carbon bonds to 14 carbon-carbon bonds, or approximately 12 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 3 turns of an α-helix, the length is equal to approximately 14 carbon-carbon bonds to 22 carbon-carbon bonds, approximately 16 carbon-carbon bonds to 20 carbon-carbon bonds, or approximately 18 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 4 turns of an α-helix, the length is equal to approximately 20 carbon-carbon bonds to 28 carbon-carbon bonds, approximately 22 carbon-carbon bonds to 26 carbon-carbon bonds, or approximately 24 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 5 turns of an α-helix, the length is equal to approximately 26 carbon-carbon bonds to 34 carbon-carbon bonds, approximately 28 carbon-carbon bonds to 32 carbon-carbon bonds, or approximately 30 carbon-carbon bonds. Where the macrocycle-forming linker spans approximately 1 turn of an α-helix, the linkage contains approximately 4 atoms to 12 atoms, approximately 6 atoms to 10 atoms, or approximately 8 atoms. Where the macrocycle-forming linker spans approximately 2 turns of the α-helix, the linkage contains approximately 7 atoms to 15 atoms, approximately 9 atoms to 13 atoms, or approximately 11 atoms. Where the macrocycle-forming linker spans approximately 3 turns of the α-helix, the linkage contains approximately 13 atoms to 21 atoms, approximately 15 atoms to 19 atoms, or approximately 17 atoms. Where the macrocycle-forming linker spans approximately 4 turns of the α-helix, the linkage contains approximately 19 atoms to 27 atoms, approximately 21 atoms to 25 atoms, or approximately 23 atoms. Where the macrocycle-forming linker spans approximately 5 turns of the α-helix, the linkage contains approximately 25 atoms to 33 atoms, approximately 27 atoms to 31 atoms, or approximately 29 atoms. Where the macrocycle-forming linker spans approximately 1 turn of the α-helix, the resulting macrocycle forms a ring containing approximately 17 members to 25 members, approximately 19 members to 23 members, or approximately 21 members. Where the macrocycle-forming linker spans approximately 2 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 29 members to 37 members, approximately 31 members to 35 members, or approximately 33 members. Where the macrocycle-forming linker spans approximately 3 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 44 members to 52 members, approximately 46 members to 50 members, or approximately 48 members. Where the macrocycle-forming linker spans approximately 4 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 59 members to 67 members, approximately 61 members to 65 members, or approximately 63 members. Where the macrocycle-forming linker spans approximately 5 turns of the α-helix, the resulting macrocycle forms a ring containing approximately 74 members to 82 members, approximately 76 members to 80 members, or approximately 78 members.

In other embodiments, provided are peptidomimetic macrocycles of Formula (IV) or (IVa):

wherein:

each A, C, D, and E is independently a natural or non-natural amino acid, and the terminal D and E independently optionally include a capping group;

B is a natural or non-natural amino acid, amino acid analog,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-];

R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or at least one of R₁ and R₂ forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids;

R₃ is hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

L is a macrocycle-forming linker of the formula -L₁-L₂-;

L₁ and L₂ are independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅;

each R₄ is alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene;

each K is O, S, SO, SO₂, CO, CO₂, or CONR₃;

each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent;

each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent;

R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅;

v and w are independently integers from 1-1000;

u is an integer from 1-10;

x, y and z are independently integers from 0-10; and

n is an integer from 1-5.

n one example, L₁ and L₂, either alone or in combination, do not form a triazole or a thioether.

In one example, at least one of R₁ and R₂ is alkyl, unsubstituted or substituted with halo-. In another example, both R₁ and R₂ are independently alkyl, unsubstituted or substituted with halo-. In some embodiments, at least one of R₁ and R₂ is methyl. In other embodiments, R₁ and R₂ are methyl.

In some embodiments, x+y+z is at least 1. In other embodiments, x+y+z is at least 2. In other embodiments, x+y+z is 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10. Each occurrence of A, B, C, D or E in a macrocycle or macrocycle precursor is independently selected. For example, a sequence represented by the formula [A], when x is 3, encompasses embodiments where the amino acids are not identical, e.g. Gln-Asp-Ala as well as embodiments where the amino acids are identical, e.g. Gln-Gln-Gln. This applies for any value of x, y, or z in the indicated ranges.

In some embodiments, the peptidomimetic macrocycle comprises a secondary structure which is an α-helix and R₈ is —H, allowing intrahelical hydrogen bonding. In some embodiments, at least one of A, B, C, D or E is an α,α-disubstituted amino acid. In one example, B is an α,α-disubstituted amino acid. For instance, at least one of A, B, C, D or E is 2-aminoisobutyric acid. In other embodiments, at least one of A, B, C, D or E is

In other embodiments, the length of the macrocycle-forming linker L as measured from a first Cα to a second Cα is selected to stabilize a desired secondary peptide structure, such as an α-helix formed by residues of the peptidomimetic macrocycle including, but not necessarily limited to, those between the first Cα to a second Cα.

Exemplary embodiments of the macrocycle-forming linker -L₁-L₂- are shown below.

Unless otherwise stated, any compounds (including peptidomimetic macrocycles, macrocycle precursors, and other compositions) are also meant to encompass compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the described structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by ¹³C- or ¹⁴C-enriched carbon are within the scope of this invention.

In some embodiments, the compounds disclosed herein can contain unnatural proportions of atomic isotopes at one or more of atoms that constitute such compounds. For example, the compounds can be radiolabeled with radioactive isotopes, such as for example tritium (³H), iodine-125 (¹²⁵I) or carbon-14 (¹⁴C). In other embodiments, one or more carbon atoms is replaced with a silicon atom. All isotopic variations of the compounds disclosed herein, whether radioactive or not, are contemplated herein.

Preparation of Peptidomimetic Macrocycles

Peptidomimetic macrocycles can be prepared by any of a variety of methods known in the art. For example, any of the residues indicated by “$” or “$r8” in Table 1, Table 1a, Table 1b, or Table 1c can be substituted with a residue capable of forming a crosslinker with a second residue in the same molecule or a precursor of such a residue.

Various methods to effect formation of peptidomimetic macrocycles are known in the art. For example, the preparation of peptidomimetic macrocycles of Formula I is described in Schafineister et al., J. Am. Chem. Soc. 122:5891-5892 (2000); Schafmeister & Verdine, J. Am. Chem. Soc. 122:5891 (2005); Walensky et al., Science 305:1466-1470 (2004); U.S. Pat. No. 7,192,713 and PCT application WO 2008/121767. The α,α-disubstituted amino acids and amino acid precursors disclosed in the cited references can be employed in synthesis of the peptidomimetic macrocycle precursor polypeptides. For example, the “S5-olefin amino acid” is (S)-α-(2′-pentenyl) alanine and the “R8 olefin amino acid” is (R)-α-(2′-octenyl) alanine. Following incorporation of such amino acids into precursor polypeptides, the terminal olefins are reacted with a metathesis catalyst, leading to the formation of the peptidomimetic macrocycle. Tn various embodiments, the following amino acids can be employed in the synthesis of the peptidomimetic macrocycle:

In other embodiments, the peptidomimetic macrocycles are of Formula IV or IVa. Methods for the preparation of such macrocycles are described, for example, in U.S. Pat. No. 7,202,332.

Additional methods of forming peptidomimetic macrocycles which are envisioned as suitable include those disclosed by Mustapa, M. Firouz Mohd et al., J. Org. Chem. (2003), 68, pp. 8193-8198; Yang, Bin et al. Bioorg Med. Chem. Lett. (2004), 14, pp. 1403-1406; U.S. Pat. No. 5,364,851; U.S. Pat. No. 5,446,128; U.S. Pat. No. 5,824,483; U.S. Pat. No. 6,713,280; and U.S. Pat. No. 7,202,332. In such embodiments, amino acid precursors are used containing an additional substituent R— at the alpha position. Such amino acids are incorporated into the macrocycle precursor at the desired positions, which can be at the positions where the crosslinker is substituted or, alternatively, elsewhere in the sequence of the macrocycle precursor. Cyclization of the precursor is then effected according to the indicated method.

Assays

The properties of peptidomimetic macrocycles are assayed, for example, by using the methods described below. In some embodiments, a peptidomimetic macrocycle has improved biological properties relative to a corresponding polypeptide lacking the substituents described herein.

Assay to Determine α-Helicity

In solution, the secondary structure of polypeptides with α-helical domains will reach a dynamic equilibrium between random coil structures and α-helical structures, often expressed as a “percent helicity”. Thus, for example, alphα-helical domains are predominantly random coils in solution, with α-helical content usually under 25%. Peptidomimetic macrocycles with optimized linkers, on the other hand, possess, for example, an alpha-helicity that is at least two-fold greater than that of a corresponding uncrosslinked polypeptide. In some embodiments, macrocycles will possess an alpha-helicity of greater than 50%. To assay the helicity of peptidomimetic macrocycles, the compounds are dissolved in an aqueous solution (e.g. 50 mM potassium phosphate solution at pH 7, or distilled H₂O, to concentrations of 25-50 μM). Circular dichroism (CD) spectra are obtained on a spectropolarimeter (e.g., Jasco J-710) using standard measurement parameters (e.g. temperature, 20° C.; wavelength, 190-260 nm; step resolution, 0.5 nm; speed, 20 nm/sec; accumulations, 10; response, 1 sec; bandwidth, 1 nm; path length, 0.1 cm). The α-helical content of each peptide is calculated by dividing the mean residue ellipticity (e.g. [Φ]222obs) by the reported value for a model helical decapeptide (Yang et al. (1986), Methods Enzymol. 130:208)).

Assay to Determine Melting Temperature (Tm).

A peptidomimetic macrocycle comprising a secondary structure such as an α-helix exhibits, for example, a higher melting temperature than a corresponding uncrosslinked polypeptide. Typically peptidomimetic macrocycles exhibit Tm of >60° C. representing a highly stable structure in aqueous solutions. To assay the effect of macrocycle formation on melting temperature, peptidomimetic macrocycles or unmodified peptides are dissolved in distilled H₂O (e.g. at a final concentration of 50 μM) and the Tm is determined by measuring the change in ellipticity over a temperature range (e.g. 4 to 95° C.) on a spectropolarimeter (e.g., Jasco J-710) using standard parameters (e.g. wavelength 222 nm; step resolution, 0.5 nm; speed, 20 nm/sec; accumulations, 10; response, 1 sec; bandwidth, 1 nm; temperature increase rate: 1° C./min; path length, 0.1 cm).

Protease Resistance Assay.

The amide bond of the peptide backbone is susceptible to hydrolysis by proteases, thereby rendering peptidic compounds vulnerable to rapid degradation in vivo. Peptide helix formation, however, typically buries the amide backbone and therefore can shield it from proteolytic cleavage. The peptidomimetic macrocycles can be subjected to in vitro trypsin proteolysis to assess for any change in degradation rate compared to a corresponding uncrosslinked polypeptide. For example, the peptidomimetic macrocycle and a corresponding uncrosslinked polypeptide are incubated with trypsin agarose and the reactions quenched at various time points by centrifugation and subsequent HPLC injection to quantitate the residual substrate by ultraviolet absorption at 280 nm Briefly, the peptidomimetic macrocycle and peptidomimetic precursor (5 meg) are incubated with trypsin agarose (Pierce) (S/E ˜125) for 0, 10, 20, 90, and 180 minutes. Reactions are quenched by tabletop centrifugation at high speed; remaining substrate in the isolated supernatant is quantified by HPLC-based peak detection at 280 nm. The proteolytic reaction displays first order kinetics and the rate constant, k, is determined from a plot of In[S] versus time (k=−1× slope).

Ex Vivo Stability Assay.

Peptidomimetic macrocycles with optimized linkers possess, for example, an ex vivo half-life that is at least two-fold greater than that of a corresponding uncrosslinked polypeptide, and possess an ex vivo half-life of 12 hours or more. For ex vivo serum stability studies, a variety of assays can be used. For example, a peptidomimetic macrocycle and a corresponding uncrosslinked polypeptide (2 meg) are incubated with fresh mouse, rat and/or human serum (2 mL) at 37° C. for 0, 1, 2, 4, 8, and 24 hours. To determine the level of intact compound, the following procedure can be used: The samples are extracted by transferring 100 μl of sera to 2 ml centrifuge tubes followed by the addition of 10 μL of 50% formic acid and 500 μL acetonitrile and centrifugation at 14,000 RPM for 10 min at 4±2° C. The supernatants are then transferred to fresh 2 ml tubes and evaporated on Turbovap under N₂<10 psi, 37° C. The samples are reconstituted in 100 μL of 50:50 acetonitrile:water and submitted to LC-MS/MS analysis.

In vitro Binding Assays.

To assess the binding and affinity of peptidomimetic macrocycles and peptidomimetic precursors to acceptor proteins, a fluorescence polarization assay (FPA) is used, for example. The FPA technique measures the molecular orientation and mobility using polarized light and fluorescent tracer. When excited with polarized light, fluorescent tracers (e.g., FITC) attached to molecules with high apparent molecular weights (e.g. FITC-labeled peptides bound to a large protein) emit higher levels of polarized fluorescence due to their slower rates of rotation as compared to fluorescent tracers attached to smaller molecules (e.g. FITC-labeled peptides that are free in solution).

For example, fluoresceinated peptidomimetic macrocycles (25 nM) are incubated with the acceptor protein (25-1000nM) in binding buffer (140 mM NaCl, 50 mM Tris-HCL, pH 7.4) for 30 minutes at room temperature. Binding activity is measured, for example, by fluorescence polarization on a luminescence spectrophotometer (e.g. Perkin-Elmer LS50B). Kd values can be determined by nonlinear regression analysis using, for example, Graphpad Prism software (GraphPad Software, Inc., San Diego, Calif.). A peptidomimetic macrocycle shows, In some embodiments, similar or lower Kd than a corresponding uncrosslinked polypeptide.

In Vitro Displacement Assays to Characterize Antagonists of Peptide-Protein Interactions.

To assess the binding and affinity of compounds that antagonize the interaction between a peptide and an acceptor protein, a fluorescence polarization assay (FPA) utilizing a fluoresceinated peptidomimetic macrocycle derived from a peptidomimetic precursor sequence is used, for example. The FPA technique measures the molecular orientation and mobility using polarized light and fluorescent tracer. When excited with polarized light, fluorescent tracers (e.g., FITC) attached to molecules with high apparent molecular weights (e.g. FITC-labeled peptides bound to a large protein) emit higher levels of polarized fluorescence due to their slower rates of rotation as compared to fluorescent tracers attached to smaller molecules (e.g. FITC-labeled peptides that are free in solution). A compound that antagonizes the interaction between the fluoresceinated peptidomimetic macrocycle and an acceptor protein will be detected in a competitive binding FPA experiment.

For example, putative antagonist compounds (1 nM to 1 mM) and a fluoresceinated peptidomimetic macrocycle (25 nM) are incubated with the acceptor protein (50 nM) in binding buffer (140 mM NaCl, 501nM Tris-HCL, pH 7.4) for 30 minutes at room temperature. Antagonist binding activity is measured, for example, by fluorescence polarization on a luminescence spectrophotometer (e.g. Perkin-Elmer LS50B). Kd values can be determined by nonlinear regression analysis using, for example, Graphpad Prism software (GraphPad Software, Inc., San Diego, Calif.).

Any class of molecule, such as small organic molecules, peptides, oligonucleotides or proteins can be examined as putative antagonists in this assay.

Assay for Protein-Ligand Binding by Affinity Selection-Mass Spectrometry

To assess the binding and affinity of test compounds for proteins, an affinity-selection mass spectrometry assay is used, for example. Protein-ligand binding experiments are conducted according to the following representative procedure outlined for a system-wide control experiment using 1 μM peptidomimetic macrocycle plus 5 μM hMDM2. A 1 μL DMSO aliquot of a 40 μM stock solution of peptidomimetic macrocycle is dissolved in 19 μL of PBS (Phosphate-buffered saline: 50 mM, pH 7.5 Phosphate buffer containing 150 mM NaCl). The resulting solution is mixed by repeated pipetting and clarified by centrifugation at 10 000 g for 10 min. To a 4 μL aliquot of the resulting supernatant is added 4 μL of 10 μM hMDM2 in PBS. Each 8.0 μL experimental sample thus contains 40 pmol (1.5 μg) of protein at 5.0 μM concentration in PBS plus 1 μM peptidomimetic macrocycle and 2.5% DMSO. Duplicate samples thus prepared for each concentration point are incubated for 60 min at room temperature, and then chilled to 4° C. prior to size-exclusion chromatography-LC-MS analysis of 5.0 μL injections. Samples containing a target protein, protein-ligand complexes, and unbound compounds are injected onto an SEC column, where the complexes are separated from non-binding component by a rapid SEC step. The SEC column eluate is monitored using UV detectors to confirm that the early-eluting protein fraction, which elutes in the void volume of the SEC column, is well resolved from unbound components that are retained on the column. After the peak containing the protein and protein-ligand complexes elutes from the primary UV detector, it enters a sample loop where it is excised from the flow stream of the SEC stage and transferred directly to the LC-MS via a valving mechanism. The (M+3H)³⁺ ion of the peptidomimetic macrocycle is observed by ESI-MS at the expected m/z, confirming the detection of the protein-ligand complex.

Assay for Protein-Ligand Kd Titration Experiments.

To assess the binding and affinity of test compounds for proteins, a protein-ligand Kd titration experiment is performed, for example. Protein-ligand K_(d) titrations experiments are conducted as follows: 2 μL DMSO aliquots of a serially diluted stock solution of titrant peptidomimetic macrocycle (5, 2.5, . . . , 0.098 mM) are prepared then dissolved in 38 μL of PBS. The resulting solutions are mixed by repeated pipetting and clarified by centrifugation at 10 000 g for 10 min. To 4.0 μL aliquots of the resulting supernatants is added 4.0 μL of 10 μM hMDM2 in PBS. Each 8.0 μL experimental sample thus contains 40 μmol (1.5 μg) of protein at 5.0 μM concentration in PBS, varying concentrations (125, 62.5, . . . , 0.24 μM) of the titrant peptide, and 2.5% DMSO. Duplicate samples thus prepared for each concentration point are incubated at room temperature for 30 min, then chilled to 4° C. prior to SEC-LC-MS analysis of 2.0 μL injections. The (M+H)¹⁺, (M+2H)²⁺, (M+3H)³⁺, and/or (M+Na)¹⁺ ion is observed by ESI-MS; extracted ion chromatograms are quantified, then fit to equations to derive the binding affinity K_(d) as described in “A General Technique to Rank Protein-Ligand Binding Affinities and Determine Allosteric vs. Direct Binding Site Competition in Compound Mixtures.” Annis, D. A.; Nazef, N.; Chuang, C. C.; Scott, M. P.; Nash, H. M. J. Am. Chem. Soc. 2004, 126, 15495-15503; also in “ALIS: An Affinity Selection-Mass Spectrometry System for the Discovery and Characterization of Protein-Ligand Interactions” D. A. Annis, C.-C. Chuang, and N. Nazef. In Mass Spectrometry in Medicinal Chemistry. Edited by Wanner K, Höfner G: Wiley-VCH; 2007:121-184. Mannhold R, Kubinyi H, Folkers G (Series Editors): Methods and Principles in Medicinal Chemistry.

Assay for Competitive Binding Experiments by Affinity Selection-Mass Spectrometry

To determine the ability of test compounds to bind competitively to proteins, an affinity selection mass spectrometry assay is performed, for example. A mixture of ligands at 40 μM per component is prepared by combining 2 μL aliquots of 400 μM stocks of each of the three compounds with 14 μL of DMSO. Then, 1 μL aliquots of this 40 μM per component mixture are combined with 1 μL DMSO aliquots of a serially diluted stock solution of titrant peptidomimetic macrocycle (10, 5, 2.5, . . . , 0.078 mM). These 2 μL samples are dissolved in 38 μL of PBS. The resulting solutions were mixed by repeated pipetting and clarified by centrifugation at 10 000 g for 10 min. To 4.0 μL aliquots of the resulting supernatants is added 4.0 μL of 10 μM hMDM2 protein in PBS. Each 8.0 μL experimental sample thus contains 40 μmol (1.5 μg) of protein at 5.0 concentration in PBS plus 0.5 μM ligand, 2.5% DMSO, and varying concentrations (125, 62.5, . . . , 0.98 μM) of the titrant peptidomimetic macrocycle. Duplicate samples thus prepared for each concentration point are incubated at room temperature for 60 min, then chilled to 4° C. prior to SEC-LC-MS analysis of 2.0 μL injections. Additional details on these and other methods are provided in “A General Technique to Rank Protein-Ligand Binding Affinities and Determine Allosteric vs. Direct Binding Site Competition in Compound Mixtures.” Annis, D. A.; Nazef, N.; Chuang, C. C.; Scott, M. P.; Nash, H. M. J. Am. Chem. Soc. 2004, 126, 15495-15503; also in “ALIS: An Affinity Selection-Mass Spectrometry System for the Discovery and Characterization of Protein-Ligand Interactions” D. A. Annis, C.-C. Chuang, and N. Nazef. In Mass Spectrometry in Medicinal Chemistry. Edited by Wanner K, Hofner G: Wiley-VCH; 2007:121-184. Mannhold R, Kubinyi H, Folkers G (Series Editors): Methods and Principles in Medicinal Chemistry.

Binding Assays in Intact Cells.

It is possible to measure binding of peptides or peptidomimetic macrocycles to their natural acceptors in intact cells by immunoprecipitation experiments. For example, intact cells are incubated with fluoresceinated (FITC-labeled) compounds for 4 hrs in the absence of scrum, followed by serum replacement and further incubation that ranges from 4-18 hrs. Cells are then pelleted and incubated in lysis buffer (50 mM Tris [pH 7.6], 150 mM NaCl, 1% CHAPS and protease inhibitor cocktail) for 10 minutes at 4° C. Extracts are centrifuged at 14,000 rpm for 15 minutes and supernatants collected and incubated with 10 μl goat anti-FITC antibody for 2 hrs, rotating at 4° C. followed by further 2 hrs incubation at 4° C. with protein A/G Sepharose (50 μl of 50% bead slurry). After quick centrifugation, the pellets are washed in lysis buffer containing increasing salt concentration (e.g., 150, 300, 500 mM). The beads are then re-equilibrated at 150 mM NaCl before addition of SDS-containing sample buffer and boiling. After centrifugation, the supernatants are optionally electrophoresed using 4%-12% gradient Bis-Tris gels followed by transfer into Immobilon-P membranes. After blocking, blots are optionally incubated with an antibody that detects FITC and also with one or more antibodies that detect proteins that bind to the peptidomimetic macrocycle.

Cellular Penetrability Assays.

A peptidomimetic macrocycle is, for example, more cell penetrable compared to a corresponding uncrosslinked macrocycle. Peptidomimetic macrocycles with optimized linkers possess, for example, cell penetrability that is at least two-fold greater than a corresponding uncrosslinked macrocycle, and often 20% or more of the applied peptidomimetic macrocycle will be observed to have penetrated the cell after 4 hours. To measure the cell penetrability of peptidomimetic macrocycles and corresponding uncrosslinked macrocycle, intact cells are incubated with fluorescently-labeled (e.g. fluoresceinated) peptidomimetic macrocycles or corresponding uncrosslinked macrocycle (10 μM) for 4 hrs in serum free media at 37° C., washed twice with media and incubated with trypsin (0.25%) for 10 min at 37° C. The cells are washed again and resuspended in PBS. Cellular fluorescence is analyzed, for example, by using either a FACSCalibur flow cytometer or Cellomics' KineticScan HCS Reader.

Cellular Efficacy Assays.

The efficacy of certain peptidomimetic macrocycles is determined, for example, in cell-based killing assays using a variety of tumorigenic and non-tumorigenic cell lines and primary cells derived from human or mouse cell populations. Cell viability is monitored, for example, over 24-96 hrs of incubation with peptidomimetic macrocycles (0.5 to 50 μM) to identify those that kill at EC₅₀<10 μM. Several standard assays that measure cell viability are commercially available and are optionally used to assess the efficacy of the peptidomimetic macrocycles. In addition, assays that measure Annexin V and caspase activation are optionally used to assess whether the peptidomimetic macrocycles kill cells by activating the apoptotic machinery. For example, the Cell Titer-glo assay is used which determines cell viability as a function of intracellular ATP concentration.

In Vivo Stability Assay.

To investigate the in vivo stability of the peptidomimetic macrocycles, the compounds are, for example, administered to mice and/or rats by IV, IP, PO or inhalation routes at concentrations ranging from 0.1 to 50 mg/kg and blood specimens withdrawn at 0′, 5′, 15′, 30′, 1 hr, 4 hrs, 8 hrs and 24 hours post-injection. Levels of intact compound in 25 μL of fresh serum are then measured by LC-MS/MS as above.

In vivo Efficacy in Animal Models.

To determine the anti-oncogenic activity of peptidomimetic macrocycles in vivo, the compounds are, for example, given alone (IP, IV, PO, by inhalation or nasal routes) or in combination with sub-optimal doses of relevant chemotherapy (e.g., cyclophosphamide, doxorubicin, etoposide). In one example, 5×10⁶ RS4; 11 cells (established from the bone marrow of a patient with acute lymphoblastic leukemia) that stably express luciferase are injected by tail vein in NOD-SCID mice 3 hrs after they have been subjected to total body irradiation. If left untreated, this form of leukemia is fatal in 3 weeks in this model. The leukemia is readily monitored, for example, by injecting the mice with D-luciferin (60 mg/kg) and imaging the anesthetized animals (e.g., Xenogen In Vivo Imaging System, Caliper Life Sciences, Hopkinton, Mass.). Total body bioluminescence is quantified by integration of photonic flux (photons/sec) by Living Image Software (Caliper Life Sciences, Hopkinton, Mass.). Peptidomimetic macrocycles alone or in combination with sub-optimal doses of relevant chemotherapeutics agents are, for example, administered to leukemic mice (10 days after injection/day 1 of experiment, in bioluminescence range of 14-16) by tail vein or IP routes at doses ranging from 0.1 mg/kg to 50 mg/kg for 7 to 21 days. Optionally, the mice are imaged throughout the experiment every other day and survival monitored daily for the duration of the experiment. Expired mice are optionally subjected to necropsy at the end of the experiment. Another animal model is implantation into NOD-SCID mice of DoHH2, a cell line derived from human follicular lymphoma, that stably expresses luciferase. These in vivo tests optionally generate preliminary pharmacokinetic, pharmacodynamic and toxicology data.

Clinical Trials.

To determine the suitability of the peptidomimetic macrocycles for treatment of humans, clinical trials are performed. For example, patients diagnosed with cancer and in need of treatment can be selected and separated in treatment and one or more control groups, wherein the treatment group is administered a peptidomimetic macrocycle, while the control groups receive a placebo or a known anti-cancer drug. The treatment safety and efficacy of the peptidomimetic macrocycles can thus be evaluated by performing comparisons of the patient groups with respect to factors such as survival and quality-of-life. In this example, the patient group treated with a peptidomimetic macrocycle can show improved long-term survival compared to a patient control group treated with a placebo.

Pharmaceutical Compositions and Routes of Administration

Pharmaceutical compositions disclosed herein include peptidomimetic macrocycles and pharmaceutically acceptable derivatives or prodrugs thereof A “pharmaceutically acceptable derivative” means any pharmaceutically acceptable salt, ester, salt of an ester, pro-drug or other derivative of a compound disclosed herein which, upon administration to a recipient, is capable of providing (directly or indirectly) a compound disclosed herein. Particularly favored pharmaceutically acceptable derivatives are those that increase the bioavailability of the compounds when administered to a mammal (e.g., by increasing absorption into the blood of an orally administered compound) or which increases delivery of the active compound to a biological compartment (e.g., the brain or lymphatic system) relative to the parent species. Some pharmaceutically acceptable derivatives include a chemical group which increases aqueous solubility or active transport across the gastrointestinal mucosa.

In some embodiments, peptidomimetic macrocycles are modified by covalently or non-covalently joining appropriate functional groups to enhance selective biological properties. Such modifications include those which increase biological penetration into a given biological compartment (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism, and alter rate of excretion.

Pharmaceutically acceptable salts of the compounds disclosed herein include those derived from pharmaceutically acceptable inorganic and organic acids and bases. Examples of suitable acid salts include acetate, adipate, benzoate, benzenesulfonate, butyrate, citrate, digluconate, dodecylsulfate, formate, fumarate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, lactate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, palmoate, phosphate, picrate, pivalate, propionate, salicylate, succinate, sulfate, tartrate, tosylate and undecanoate. Salts derived from appropriate bases include alkali metal (e.g., sodium), alkaline earth metal (e.g., magnesium), ammonium and N-(alkyl)₄ ⁺ salts.

For preparing pharmaceutical compositions from the compounds disclosed herein, pharmaceutically acceptable carriers include either solid or liquid carriers. Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules. A solid carrier can be one or more substances, which also acts as diluents, flavoring agents, binders, preservatives, tablet disintegrating agents, or an encapsulating material. Details on techniques for formulation and administration are well described in the scientific and patent literature, see, e.g., the latest edition of Remington's Pharmaceutical Sciences, Maack Publishing Co, Easton Pa.

In powders, the carrier is a finely divided solid, which is in a mixture with the finely divided active component. In tablets, the active component is mixed with the carrier having the necessary binding properties in suitable proportions and compacted in the shape and size desired.

Suitable solid excipients are carbohydrate or protein fillers include, but are not limited to sugars, including lactose, sucrose, mannitol, or sorbitol; starch from corn, wheat, rice, potato, or other plants; cellulose such as methyl cellulose, hydroxypropylmethyl-cellulose, or sodium carboxymethylcellulose; and gums including arabic and tragacanth; as well as proteins such as gelatin and collagen. If desired, disintegrating or solubilizing agents are added, such as the cross-linked polyvinyl pyrrolidone, agar, alginic acid, or a salt thereof, such as sodium alginate.

Liquid form preparations include solutions, suspensions, and emulsions, for example, water or water/propylene glycol solutions. For parenteral injection, liquid preparations can be formulated in solution in aqueous polyethylene glycol solution.

The pharmaceutical preparation can be in unit dosage form. In such form the preparation is subdivided into unit doses containing appropriate quantities of the active component. The unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, such as packeted tablets, capsules, and powders in vials or ampoules. Also, the unit dosage form can be a capsule, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.

When one or more compositions disclosed herein comprise a combination of a peptidomimetic macrocycle and one or more additional therapeutic or prophylactic agents, both the compound and the additional agent should be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen. In some embodiments, the additional agents are administered separately, as part of a multiple dose regimen, from one or more compounds disclosed herein. Alternatively, those agents are part of a single dosage form, mixed together with the compounds disclosed herein in a single composition.

Methods of Use

In one aspect, provided herein are novel peptidomimetic macrocycles that are useful in competitive binding assays to identify agents which bind to the natural ligand(s) of the proteins or peptides upon which the peptidomimetic macrocycles are modeled. For example, in the p53/MDMX system, labeled peptidomimetic macrocycles based on p53 can be used in a MDMX binding assay along with small molecules that competitively bind to MDMX. Competitive binding studies allow for rapid in vitro evaluation and determination of drug candidates specific for the p53/MDMX system. Such binding studies can be performed with any of the peptidomimetic macrocycles disclosed herein and their binding partners.

Further provided are methods for the generation of antibodies against the peptidomimetic macrocycles. In some embodiments, these antibodies specifically bind both the peptidomimetic macrocycle and the precursor peptides, such as p53, to which the peptidomimetic macrocycles are related. Such antibodies, for example, disrupt the native protein-protein interaction, for example, binding between p53 and MDMX.

In other aspects, provided herein are both prophylactic and therapeutic methods of treating a subject at risk of (or susceptible to) a disorder or having a disorder associated with aberrant (e.g., insufficient or excessive) expression or activity of the molecules including p53, MDM2 or MDMX.

In another embodiment, a disorder is caused, at least in part, by an abnormal level of p53 or MDM2 or MDMX, (e.g., over or under expression), or by the presence of p53 or MDM2 or MDMX exhibiting abnormal activity. As such, the reduction in the level and/or activity of p53 or MDM2 or MDMX, or the enhancement of the level and/or activity of p53 or MDM2 or MDMX, by peptidomimetic macrocycles derived from p53, is used, for example, to ameliorate or reduce the adverse symptoms of the disorder.

In another aspect, provided herein are methods for treating or preventing a disease including hyperproliferative disease and inflammatory disorder by interfering with the interaction or binding between binding partners, for example, between p53 and MDM2 or p53 and MDMX. These methods comprise administering an effective amount of a compound to a warm blooded animal, including a human. In some embodiments, the administration of one or more compounds disclosed herein induces cell growth arrest or apoptosis.

As used herein, the term “treatment” is defined as the application or administration of a therapeutic agent to a patient, or application or administration of a therapeutic agent to an isolated tissue or cell line from a patient, who has a disease, a symptom of disease or a predisposition toward a disease, with the purpose to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve or affect the disease, the symptoms of disease or the predisposition toward disease.

In some embodiments, the peptidomimetic macrocycles can be used to treat, prevent, and/or diagnose cancers and neoplastic conditions. As used herein, the terms “cancer”, “hyperproliferative” and “neoplastic” refer to cells having the capacity for autonomous growth, i.e., an abnormal state or condition characterized by rapidly proliferating cell growth. Hyperproliferative and neoplastic disease states can be categorized as pathologic, i.e., characterizing or constituting a disease state, or can be categorized as non-pathologic, i.e., a deviation from normal but not associated with a disease state. The term is meant to include all types of cancerous growths or oncogenic processes, metastatic tissues or malignantly transformed cells, tissues, or organs, irrespective of histopathologic type or stage of invasiveness. A metastatic tumor can arise from a multitude of primary tumor types, including but not limited to those of breast, lung, liver, colon and ovarian origin. “Pathologic hyperproliferative” cells occur in disease states characterized by malignant tumor growth. Examples of non-pathologic hyperproliferative cells include proliferation of cells associated with wound repair. Examples of cellular proliferative and/or differentiative disorders include cancer, e.g., carcinoma, sarcoma, or metastatic disorders. In some embodiments, the peptidomimetic macrocycles are novel therapeutic agents for controlling breast cancer, ovarian cancer, colon cancer, lung cancer, metastasis of such cancers and the like.

Examples of cancers or neoplastic conditions include, but are not limited to, a fibrosarcoma, myosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, gastric cancer, esophageal cancer, rectal cancer, pancreatic cancer, ovarian cancer, prostate cancer, uterine cancer, cancer of the head and neck, skin cancer, brain cancer, squamous cell carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinoma, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testicular cancer, small cell lung carcinoma, non-small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, meningioma, melanoma, neuroblastoma, retinoblastoma, leukemia, lymphoma, or Kaposi sarcoma.

In some embodiments, the cancer is head and neck cancer, melanoma, lung cancer, breast cancer, or glioma.

Examples of proliferative disorders include hematopoietic neoplastic disorders. As used herein, the term “hematopoietic neoplastic disorders” includes diseases involving hyperplastic/neoplastic cells of hematopoietic origin, e.g., arising from myeloid, lymphoid or erythroid lineages, or precursor cells thereof. The diseases can arise from poorly differentiated acute leukemias, e.g., erythroblastic leukemia and acute megakaryoblastic leukemia. Additional exemplary myeloid disorders include, but are not limited to, acute promyeloid leukemia (APML), acute myelogenous leukemia (AML) and chronic myelogenous leukemia (CML) (reviewed in Vaickus (1991), Crit. Rev. Oncol./Hemotol. 11:267-97); lymphoid malignancies include, but are not limited to acute lymphoblastic leukemia (ALL) which includes B-lineage ALL and T-lineage ALL, chronic lymphocytic leukemia (CLL), prolymphocytic leukemia (PLL), hairy cell leukemia (HLL) and Waldenstrom's macroglobulinemia (WM). Additional forms of malignant lymphomas include, but are not limited to non-Hodgkin lymphoma and variants thereof, peripheral T cell lymphomas, adult T cell leukemia/lymphoma (ATL), cutaneous T-cell lymphoma (CTCL), large granular lymphocytic leukemia (LGF), Hodgkin's disease and Reed-Stemberg disease.

Examples of cellular proliferative and/or differentiative disorders of the breast include, but are not limited to, proliferative breast disease including, e.g., epithelial hyperplasia, sclerosing adenosis, and small duct papillomas; tumors, e.g., stromal tumors such as fibroadenoma, phyllodes tumor, and sarcomas, and epithelial tumors such as large duct papilloma; carcinoma of the breast including in situ (noninvasive) carcinoma that includes ductal carcinoma in situ (including Paget's disease) and lobular carcinoma in situ, and invasive (infiltrating) carcinoma including, but not limited to, invasive ductal carcinoma, invasive lobular carcinoma, medullary carcinoma, colloid (mucinous) carcinoma, tubular carcinoma, and invasive papillary carcinoma, and miscellaneous malignant neoplasms. Disorders in the male breast include, but are not limited to, gynecomastia and carcinoma.

Examples of cellular proliferative and/or differentiative disorders of the skin include, but are not limited to proliferative skin disease such as melanomas, including mucosal melanoma, superficial spreading melanoma, nodular melanoma, lentigo (e.g. lentigo maligna, lentigo maligna melanoma, or acral lentiginous melanoma), amelanotic melanoma, desmoplastic melanoma, melanoma with features of a Spitz nevus, melanoma with small nevus-like cells, polypoid melanoma, and soft-tissue melanoma; basal cell carcinomas including micronodular basal cell carcinoma, superficial basal cell carcinoma, nodular basal cell carcinoma (rodent ulcer), cystic basal cell carcinoma, cicatricial basal cell carcinoma, pigmented basal cell carcinoma, aberrant basal cell carcinoma, infiltrative basal cell carcinoma, nevoid basal cell carcinoma syndrome, polypoid basal cell carcinoma, pore-like basal cell carcinoma, and fibroepithelioma of Pinkus; squamus cell carcinomas including acanthoma (large cell acanthoma), adenoid squamous cell carcinoma, basaloid squamous cell carcinoma, clear cell squamous cell carcinoma, signet-ring cell squamous cell carcinoma, spindle cell squamous cell carcinoma, Marjolin's ulcer, erythroplasia of Queyrat, and Bowen's disease; or other skin or subcutaneous tumors.

Examples of cellular proliferative and/or differentiative disorders of the lung include, but are not limited to, bronchogenic carcinoma, including paraneoplastic syndromes, bronchioloalveolar carcinoma, neuroendocrine tumors, such as bronchial carcinoid, miscellaneous tumors, and metastatic tumors; pathologies of the pleura, including inflammatory pleural effusions, noninflammatory pleural effusions, pneumothorax, and pleural tumors, including solitary fibrous tumors (pleural fibroma) and malignant mesothelioma.

Examples of cellular proliferative and/or differentiative disorders of the colon include, but are not limited to, non-neoplastic polyps, adenomas, familial syndromes, colorectal carcinogenesis, colorectal carcinoma, and carcinoid tumors.

Examples of cellular proliferative and/or differentiative disorders of the liver include, but are not limited to, nodular hyperplasias, adenomas, and malignant tumors, including primary carcinoma of the liver and metastatic tumors.

Examples of cellular proliferative and/or differentiative disorders of the ovary include, but are not limited to, ovarian tumors such as, tumors of coelomic epithelium, serous tumors, mucinous tumors, endometrioid tumors, clear cell adenocarcinoma, cystadenofibroma, Brenner tumor, surface epithelial tumors; germ cell tumors such as mature (benign) teratomas, monodermal teratomas, immature malignant teratomas, dysgerminoma, endodermal sinus tumor, choriocarcinoma; sex cord-stomal tumors such as, granulosa-theca cell tumors, thecomafibromas, androblastomas, hill cell tumors, and gonadoblastoma; and metastatic tumors such as Krukenberg tumors.

While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments described herein can be employed in practicing the invention. It is intended that the following claims define the scope and that methods and structures within the scope of these claims and their equivalents be covered thereby.

EXAMPLES Example 1 Synthesis of 6-chlorotryptophan Fmoc amino acids

Tert-butyl 6-chloro-3-formyl-1H-indole-1-carboxylate, 1. To a stirred solution of dry DMF (12 mL) was added dropwise POCl₃ (3.92 mL, 43 mmol, 1.3 equiv) at 0° C. under Argon. The solution was stirred at the same temperature for 20 min before a solution of 6-chloroindole (5.0 g, 33 mmol, 1 eq.) in dry DMF (30 mL) was added dropwise. The resulting mixture was allowed to warm to room temperature and stirred for an additional 2.5 h. Water (50 mL) was added and the solution was neutralized with 4M aqueous NaOH (pH ˜8). The resulting solid was filtered off, washed with water and dried under vacuum. This material was directly used in the next step without additional purification. To a stirred solution of the crude formyl indole (33 mmol, 1 eq.) in THF (150 mL) was added successively Boc₂O (7.91 g, 36.3 mmol, 1.1 equiv) and DMAP (0.4 g, 3.3 mmol, 0.1 equiv) at room temperature under N₂. The resulting mixture was stirred at room temperature for 1.5 h and the solvent was evaporated under reduced pressure. The residue was taken up in EtOAc and washed with 1N HCl, dried and concentrated to give the formyl indole 1 (9 g, 98% over 2 steps) as a white solid. ¹H NMR (CDCl₃) δ: 1.70 (s, Boc, 9H); 7.35 (dd, 1H); 8.21 (m, 3H); 10.07 (s, 1H).

Tert-butyl 6-chloro-3-(hydroxymethyl)-1H-indole-1-carboxylate, 2. To a solution of compound 1 (8.86 g, 32 mmol, 1 eq.) in ethanol (150 mL) was added NaBH₄ (2.4 g, 63 mmol, 2 eq.). The reaction was stirred for 3 h at room temperature. The reaction mixture was concentrated and the residue was poured into diethyl ether and water. The organic layer was separated, dried over magnesium sulfate and concentrated to give a white solid (8.7 g, 98%). This material was directly used in the next step without additional purification. ¹H NMR (CDCl₃) δ: 1.65 (s, Boc, 9H); 4.80 (s, 2H, CH₂); 7.21 (dd, 1H); 7.53 (m, 2H); 8.16 (bs, 1H).

Tert-butyl 3-(bromomethyl)-6-chloro-1H-indole-1-carboxylate, 3. To a solution of compound 2 (4.1 g, 14.6 mmol, 1 eq.) in dichloromethane (50 mL) under argon was added a solution of triphenylphosphine (4.59 g, 17.5 mmol, 1.2 eq.) in dichloromethane (50 mL) at −40° C. The reaction solution was stirred an additional 30 min at 40° C. Then NBS (3.38 g, 19 mmol, 1.3 eq.) was added. The resulting mixture was allowed to warm to room temperature and stirred overnight. Dichloromethane was evaporated, Carbon Tetrachloride (100 mL) was added and the mixture was stirred for 1 h and filtrated. The filtrate was concentrated, loaded in a silica plug and quickly eluted with 25% EtOAc in Hexanes. The solution was concentrated to give a white foam (3.84 g, 77%). ¹H NMR (CDCl₃) δ: 1.66 (s, Boc, 9H); 4.63 (s, 2H, CH₂); 7.28 (dd, 1H); 7.57 (d, 1H); 7.64 (bs, 1H); 8.18 (bs, 1H).

αMe-6Cl-Trp(Boc)-Ni—S-BPB, 4. To S-Ala-Ni—S-BPB (2.66 g, 5.2 mmol, 1 eq.) and KO-tBu (0.87 g, 7.8 mmol, 1.5 eq.) was added 50 mL of DMF under argon. The bromide derivative compound 3 (2.68 g, 7.8 mmol, 1.5 eq.) in solution of DMF (5.0 mL) was added via syringe. The reaction mixture was stirred at ambient temperature for 1 h. The solution was then quenched with 5% aqueous acetic acid and diluted with water. The desired product was extracted in dichloromethane, dried and concentrated. The oily product 4 was purified by flash chromatography (solid loading) on normal phase using EtOAc and Hexanes as eluents to give a red solid (1.78 g, 45% yield). aMe-6Cl-Trp(Boc)-Ni—S-BPB, 4: M+H calc. 775.21, M+H obs. 775.26; ¹H NMR (CDCl₃) δ: 1.23 (s, 3H, aMe); 1.56 (m, 11H, Boc+CH₂); 1.82-2.20 (m, 4H, 2CH₂); 3.03 (m, 1H, CH_(α)); 3.24 (m, 2H, CH₂); 3.57 and 4.29 (AB system, 2H, CH₂ (benzyl), 12.8 Hz); 6.62 (d, 2H); 6.98 (d, 1H); 7.14 (m, 2H); 7.23 (m, 1H); 7.32-7.36 (m, 5H); 7.50 (m, 2H); 7.67 (bs, 1H); 7.98 (d, 2H); 8.27 (m, 2H).

Fmoc-αMe-6Cl-Trp(Boc)-OH, 6. To a solution of 3N HCl/MeOH (⅓, 15 mL) at 50° C. was added a solution of compound 4 (1.75 g, 2.3 mmol, 1 eq.) in MeOH (5 ml) dropwise. The starting material disappeared within 3-4 h. The acidic solution was then cooled to 0° C. with an ice bath and quenched with an aqueous solution of Na₂CO₃ (1.21 g, 11.5 mmol, 5 eq.). Methanol was removed and 8 more equivalents of Na₇CO₃ (1.95 g, 18.4 mmol) were added to the suspension. The Nickel scavenging EDTA disodium salt dihydrate (1.68 g, 4.5 mmol, 2 eq.) was then added and the suspension was stirred for 2 h. A solution of Fmoc-OSu (0.84 g, 2.5 mmol, 1.1 eq.) in acetone (50 mL) was added and the reaction was stirred overnight. Afterwards, the reaction was diluted with diethyl ether and 1N HCl. The organic layer was then dried over magnesium sulfate and concentrated in vacuo. The desired product 6 was purified on normal phase using acetone and dichloromethane as eluents to give a white foam (0.9 g, 70% yield). Fmoc-aMe-6Cl-Trp(Boc)-OH, 6: M+H calc. 575.19, M+H obs. 575.37; ¹H NMR (CDCl₃) 1.59 (s, 9H, Boc); 1.68 (s, 3H, Me); 3.48 (bs, 2H, CH₂); 4.22 (m, 1H, CH); 4.39 (bs, 2H, CH₂); 5.47 (s, 1H, NH); 7.10 (m, 1H); 7.18 (m, 2H); 7.27 (m, 2H); 7.39 (m, 2H); 7.50 (m, 2H); 7.75 (d, 2H); 8.12 (bs, 1H).

6Cl-Trp(Boc)-Ni—S-BPB, 5. To Gly-Ni—S-BPB (4.6 g, 9.2 mmol, 1 eq.) and KO-tBu (1.14 g, 10.1 mmol, 1.1 eq.) was added 95 mL of DMF under argon. The bromide derivative compound 3 (3.5 g, 4.6 mmol, 1.1 eq.) in solution of DMF (10 mL) was added via syringe. The reaction mixture was stirred at ambient temperature for 1 h. The solution was then quenched with 5% aqueous acetic acid and diluted with water. The desired product was extracted in dichloromethane, dried and concentrated. The oily product 5 was purified by flash chromatography (solid loading) on normal phase using EtOAc and Hexanes as eluents to give a red solid (5 g, 71% yield). 6Cl-Trp(Boc)-Ni—S-BPB, 5: M+H calc. 761.20, M+H obs. 761.34; ¹H NMR (CDCl₃) δ: 1.58 (m, 11H, Boc+CH₂); 1.84 (m, 1H); 1.96 (m, 1H); 2.24 (m, 2H, CH₂); 3.00 (m, 1H, CH_(α)); 3.22 (m, 2H, CH₂); 3.45 and 4.25 (AB system, 2H, CH₂ (benzyl), J=12.8 Hz); 4.27 (m, 1H, CH_(α)); 6.65 (d, 2H); 6.88 (d, 1H); 7.07 (m, 2H); 7.14 (m, 2H); 7.28 (m, 3H); 7.35-7.39 (m, 2H); 7.52 (m, 2H); 7.96 (d, 2H); 8.28 (m, 2H).

Fmoc-6Cl-Trp(Boc)-OH, 7. To a solution of 3N HCl/MeOH (⅓, 44 mL) at 50° C. was added a solution of compound 5 (5 g, 6.6 mmol, 1 eq.) in MeOH (10 ml) dropwise. The starting material disappeared within 3-4 h. The acidic solution was then cooled to 0° C. with an ice bath and quenched with an aqueous solution of Na₂CO₃ (3.48 g, 33 mmol, 5 eq.). Methanol was removed and 8 more equivalents of Na₂CO₃ (5.57 g, 52 mmol) were added to the suspension. The Nickel scavenging EDTA disodium salt dihydrate (4.89 g, 13.1 mmol, 2 eq.) and the suspension was stirred for 2 h. A solution of Fmoc-OSu (2.21 g, 6.55 mmol, 1.1 eq.) in acetone (100 mL) was added and the reaction was stirred overnight. Afterwards, the reaction was diluted with diethyl ether and 1N HCl. The organic layer was then dried over magnesium sulfate and concentrated in vacuo. The desired product 7 was purified on normal phase using acetone and dichloromethane as eluents to give a white foam (2.6 g, 69% yield). Fmoc-6Cl-Trp(Boc)-OH, 7: M+H calc. 561.17, M+H obs. 561.37; ¹H NMR (CDCl₃) 1.63 (s, 9H, Boc); 3.26 (m, 2H, CH₂); 4.19 (m, 1H, CH); 4.39 (m, 2H, CH₂); 4.76 (m, 1H); 5.35 (d, 1H, NH); 7.18 (m, 2H); 7.28 (m, 2H); 7.39 (m, ³H); 7.50 (m, 2H); 7.75 (d, 2H); 8.14 (bs, 1H).

Example 2 Peptidomimetic Macrocycles

Peptidomimetic macrocycles were synthesized, purified and analyzed as previously described and as described below (Schafineister et al., J. Am. Chem. Soc. 122:5891-5892 (2000); Schameister & Verdine, J. Am. Chem. Soc. 122:5891 (2005); Walensky et al., Science 305:1466-1470 (2004); and U.S. Pat. No. 7,192,713). Peptidomimetic macrocycles were designed by replacing two or more naturally occurring amino acids with the corresponding synthetic amino acids. Substitutions were made at i and i+4, and i and i+7 positions. Peptide synthesis was performed either manually or on an automated peptide synthesizer (Applied Biosystems, model 433A), using solid phase conditions, rink amide AM resin (Novabiochem), and Fmoc main-chain protecting group chemistry. For the coupling of natural Fmoc-protected amino acids (Novabiochem), 10 equivalents of amino acid and a 1:1:2 molar ratio of coupling reagents HBTU/HOBt (Novabiochem)/DIEA were employed. Non-natural amino acids (4 equiv) were coupled with a 1:1:2 molar ratio of HATU (Applied Biosystems)/HOBt/DIEA. The N-termini of the synthetic peptides were acetylated, while the C-termini were amidated.

Purification of cross-linked compounds was achieved by high performance liquid chromatography (HPLC) (Varian ProStar) on a reverse phase C18 column (Varian) to yield the pure compounds. Chemical composition of the pure products was confirmed by LC/MS mass spectrometry (Micromass LCT interfaced with Agilent 1100 HPLC system) and amino acid analysis (Applied Biosystems, model 420A).

The following protocol was used in the synthesis of dialkyne-crosslinked peptidomimetic macrocycles, including SP662, SP663 and SP664. Fully protected resin-bound peptides were synthesized on a PEG-PS resin (loading 0.45 mmol/g) on a 0.2 mmol scale. Deprotection of the temporary Fmoc group was achieved by 3×10 min treatments of the resin bound peptide with 20% (v/v) piperidine in DMF. After washing with NMP (3×), dichloromethane (3×) and NMP (3×), coupling of each successive amino acid was achieved with 1×60 min incubation with the appropriate preactivated Fmoc-amino acid derivative. All protected amino acids (0.4 mmol) were dissolved in NMP and activated with HCTU (0.4 mmol) and DIEA (0.8 mmol) prior to transfer of the coupling solution to the deprotected resin-bound peptide. After coupling was completed, the resin was washed in preparation for the next deprotection/coupling cycle. Acetylation of the amino terminus was carried out in the presence of acetic anhydride/DIEA in NMP. The LC-MS analysis of a cleaved and deprotected sample obtained from an aliquot of the fully assembled resin-bound peptide was accomplished in order to verifying the completion of each coupling. In a typical example, tetrahydrofuran (4 ml) and triethylamine (2 ml) were added to the peptide resin (0.2 mmol) in a 40 ml glass vial and shaken for 10 minutes. Pd(PPh₃)₂Cl₂ (0.014 g, 0.02 mmol) and copper iodide (0.008 g, 0.04 mmol) were then added and the resulting reaction mixture was mechanically shaken 16 hours while open to atmosphere. The diyne-cyclized resin-bound peptides were deprotected and cleaved from the solid support by treatment with TFA/H₂O/TIS (95/5/5 v/v) for 2.5 h at room temperature. After filtration of the resin the TFA solution was precipitated in cold diethyl ether and centrifuged to yield the desired product as a solid. The crude product was purified by preparative HPLC.

The following protocol was used in the synthesis of single alkyne-crosslinked peptidomimetic macrocycles, including SP665. Fully protected resin-bound peptides were synthesized on a Rink amide MBHA resin (loading 0.62 mmol/g) on a 0.1 mmol scale. Deprotection of the temporary Fmoc group was achieved by 2×20 min treatments of the resin bound peptide with 25% (v/v) piperidine in NMP. After extensive flow washing with NMP and dichloromethane, coupling of each successive amino acid was achieved with 1×60 min incubation with the appropriate preactivated Fmoc-amino acid derivative. All protected amino acids (1 mmol) were dissolved in NMP and activated with HCTU (1 mmol) and DIEA (1 mmol) prior to transfer of the coupling solution to the deprotected resin-bound peptide. After coupling was completed, the resin was extensively flow washed in preparation for the next deprotection/coupling cycle. Acetylation of the amino terminus was carried out in the presence of acetic anhydride/DIEA in NMP/NMM. The LC-MS analysis of a cleaved and deprotected sample obtained from an aliquot of the fully assembled resin-bound peptide was accomplished in order to verifying the completion of each coupling. In a typical example, the peptide resin (0.1 mmol) was washed with DCM. Resin was loaded into a microwave vial. The vessel was evacuated and purged with nitrogen. Molybdenumhexacarbonyl (0.01 eq, Sigma Aldrich 199959) was added. Anhydrous chlorobenzene was added to the reaction vessel. Then 2-fluorophenol (1 eq, Sigma Aldrich F12804) was added. The reaction was then loaded into the microwave and held at 130° C. for 10 minutes. Reaction may need to be pushed a subsequent time for completion. The alkyne metathesized resin-bound peptides were deprotected and cleaved from the solid support by treatment with TFA/H₂O/TIS (94/3/3 v/v) for 3 h at room temperature. After filtration of the resin the TFA solution was precipitated in cold diethyl ether and centrifuged to yield the desired product as a solid. The crude product was purified by preparative HPLC.

Table 1 shows a list of peptidomimetic macrocycles prepared.

TABLE 1 SEQ ID Iso- Exact Found Calc Calc Calc SP Sequence NO: mer Mass Mass (M + 1)/1 (M + 2)/2 (M + 3)/3 SP1 Ac-F$r8AYWEAc3cL$AAA-NH2 10 1456.78 729.44 1457.79 729.4 486.6 SP2 Ac-F$r8AYWEAc3cL$AAibA-NH2 11 1470.79 736.4 1471.8 736.4 491.27 SP3 Ac-LTF$r8AYWAQL$SANle-NH2 12 1715.97 859.02 1716.98 858.99 573 SP4 Ac-LTF$r8AYWAQL$SAL-NH2 13 1715.97 859.02 1716.98 858.99 573 SP5 Ac-LTF$r8AYWAQL$SAM-NH2 14 1733.92 868.48 1734.93 867.97 578.98 SP6 Ac-LTF$r8AYWAQL$SAhL-NH2 15 1729.98 865.98 1730.99 866 577.67 SP7 Ac-LTF$r8AYWAQL$SAF-NH2 16 1749.95 876.36 1750.96 875.98 584.32 SP8 Ac-LTF$r8AYWAQL$SAI-NH2 17 1715.97 859.02 1716.98 858.99 573 SP9 Ac-LTF$r8AYWAQL$SAChg-NH2 18 1741.98 871.98 1742.99 872 581.67 SP10 Ac-LTF$r8AYWAQL$SAAib-NH2 19 1687.93 845.36 1688.94 844.97 563.65 SP11 Ac-LTF$r8AYWAQL$SAA-NH2 20 1673.92 838.01 1674.93 837.97 558.98 SP12 Ac-LTF$r8AYWA$L$S$Nle-NH2 21 1767.04 884.77 1768.05 884.53 590.02 SP13 Ac-LTF$r8AYWA$L$S$A-NH2 22 1724.99 864.23 1726 863.5 576 SP14 Ac-F$r8AYWEAc3cL$AANle-NH2 23 1498.82 750.46 1499.83 750.42 500.61 SP15 Ac-F$r8AYWEAc3cL$AAL-NH2 24 1498.82 750.46 1499.83 750.42 500.61 SP16 Ac-F$r8AYWEAc3cL$AAM-NH2 25 1516.78 759.41 1517.79 759.4 506.6 SP17 Ac-F$r8AYWEAc3cL$AAhL-NH2 26 1512.84 757.49 1513.85 757.43 505.29 SP18 Ac-F$r8AYWEAc3cL$AAF-NH2 27 1532.81 767.48 1533.82 767.41 511.94 SP19 Ac-F$r8AYWEAc3cL$AAI-NH2 28 1498.82 750.39 1499.83 750.42 500.61 SP20 Ac-F$r8AYWEAc3cL$AAChg-NH2 29 1524.84 763.48 1525.85 763.43 509.29 SP21 Ac-F$r8AYWEAc3cL$AACha-NH2 30 1538.85 770.44 1539.86 770.43 513.96 SP22 Ac-F$r8AYWEAc3cL$AAAib-NH2 31 1470.79 736.84 1471.8 736.4 491.27 SP23 Ac-LTF$r8AYWAQL$AAAibV-NH2 32 1771.01 885.81 1772.02 886.51 591.34 SP24 Ac-LTF$r8AYWAQL$AAAibV-NH2 33 iso2 1771.01 886.26 1772.02 886.51 591.34 SP25 Ac-LTF$r8AYWAQL$SAibAA-NH2 34 1758.97 879.89 1759.98 880.49 587.33 SP26 Ac-LTF$r8AYWAQL$SAibAA-NH2 35 iso2 1758.97 880.34 1759.98 880.49 587.33 SP27 Ac-HLTF$r8HHWHQL$AANleNle-NH2 36 2056.15 1028.86 2057.16 1029.08 686.39 SP28 Ac-DLTF$r8HHWHQL$RRLV-NH2 37 2190.23 731.15 2191.24 1096.12 731.08 SP29 Ac-HHTF$r8HHWHQL$AAML-NH2 38 2098.08 700.43 2099.09 1050.05 700.37 SP30 Ac-F$r8HHWHQL$RRDCha-NH2 39 1917.06 959.96 1918.07 959.54 640.03 SP31 Ac-F$r8HHWHQL$HRFV-NH2 40 1876.02 938.65 1877.03 939.02 626.35 SP32 Ac-HLTF$r8HHWHQL$AAhLA-NH2 41 2028.12 677.2 2029.13 1015.07 677.05 SP33 Ac-DLTF$r8HHWHQL$RRChgl-NH2 42 2230.26 1115.89 2231.27 1116.14 744.43 SP34 Ac-DLTF$r8HHWHQL$RRChgl-NH2 43 iso2 2230.26 1115.96 2231.27 1116.14 744.43 SP35 Ac-HHTF$r8HHWHQL$AAChav-NH2 44 2106.14 1053.95 2107.15 1054.08 703.05 SP36 Ac-F$r8HHWHQL$RRDa-NH2 45 1834.99 918.3 1836 918.5 612.67 SP37 Ac-F$r8HHWHQL$HRAibG-NH2 46 1771.95 886.77 1772.96 886.98 591.66 SP38 Ac-F$r8AYWAQL$HHNleL-NH2 47 1730.97 866.57 1731.98 866.49 578 SP39 Ac-F$r8AYWSAL$HQANle-NH2 48 1638.89 820.54 1639.9 820.45 547.3 SP40 Ac-F$r8AYWVQL$QHChgl-NH2 49 1776.01 889.44 1777.02 889.01 593.01 SP41 Ac-F$r8AYWTAL$QQNlev-NH2 50 1671.94 836.97 1672.95 836.98 558.32 SP42 Ac-F$r8AYWYQL$HAibAa-NH2 51 1686.89 844.52 1687.9 844.45 563.3 SP43 Ac-LTF$r8AYWAQL$HHLa-NH2 52 1903.05 952.27 1904.06 952.53 635.36 SP44 Ac-LTF$r8AYWAQL$HHLa-NH2 53 iso2 1903.05 952.27 1904.06 952.53 635.36 SP45 Ac-LTF$r8AYWAQL$HQNlev-NH2 54 1922.08 962.48 1923.09 962.05 641.7 SP46 Ac-LTF$r8AYWAQL$HQNlev-NH2 55 iso2 1922.08 962.4 1923.09 962.05 641.7 SP47 Ac-LTF$r8AYWAQL$QQMl-NH2 56 1945.05 973.95 1946.06 973.53 649.36 SP48 Ac-LTF$r8AYWAQL$QQMl-NH2 57 iso2 1945.05 973.88 1946.06 973.53 649.36 SP49 Ac-LTF$r8AYWAQL$HAibhLV-NH2 58 1893.09 948.31 1894.1 947.55 632.04 SP50 Ac-LTF$r8AYWAQL$AHFA-NH2 59 1871.01 937.4 1872.02 936.51 624.68 SP51 Ac-HLTF$r8HHWHQL$AANlel-NH2 60 2056.15 1028.79 2057.16 1029.08 686.39 SP52 Ac-DLTF$r8HHWHQL$RRLa-NH2 61 2162.2 721.82 2163.21 1082.11 721.74 SP53 Ac-HHTF$r8HHWHQL$AAMv-NH2 62 2084.07 1042.92 2085.08 1043.04 695.7 SP54 Ac-F$r8HHWHQL$RRDA-NH2 63 1834.99 612.74 1836 918.5 612.67 SP55 Ac-F$r8HHWHQL$HRFCha-NH2 64 1930.06 966.47 1931.07 966.04 644.36 SP56 Ac-F$r8AYWEAL$AA-NHAm 65 1443.82 1445.71 1444.83 722.92 482.28 SP57 Ac-F$r8AYWEAL$AA-NHiAm 66 1443.82 723.13 1444.83 722.92 482.28 SP58 Ac-F$r8AYWEAL$AA-NHnPr3Ph 67 1491.82 747.3 1492.83 746.92 498.28 SP59 Ac-F$r8AYWEAL$AA-NHnBu33Me 68 1457.83 1458.94 1458.84 729.92 486.95 SP60 Ac-F$r8AYWEAL$AA-NHnPr 69 1415.79 709.28 1416.8 708.9 472.94 SP61 Ac-F$r8AYWEAL$AA-NHnEt2Ch 70 1483.85 1485.77 1484.86 742.93 495.62 SP62 Ac-F$r8AYWEAL$AA-NHnEt2Cp 71 1469.83 1470.78 1470.84 735.92 490.95 SP63 Ac-F$r8AYWEAL$AA-NHHex 72 1457.83 730.19 1458.84 729.92 486.95 SP64 Ac-LTF$r8AYWAQL$AAIA-NH2 73 1771.01 885.81 1772.02 886.51 591.34 SP65 Ac-LTF$r8AYWAQL$AAIA-NH2 74 iso2 1771.01 866.8 1772.028 86.51 591.34 SP66 Ac-LTF$r8AYWAAL$AAMA-NH2 75 1731.94 867.08 1732.95 866.98 578.32 SP67 Ac-LTF$r8AYWAAL$AAMA-NH2 76 iso2 1731.94 867.28 1732.95 866.98 578.32 SP68 Ac-LTF$r8AYWAQL$AANleA-NH2 77 1771.01 867.1 1772.02 886.51 591.34 SP69 Ac-LTF$r8AYWAQL$AANleA-NH2 78 iso2 1771.01 886.89 1772.02 886.51 591.34 SP70 Ac-LTF$r8AYWAQL$AAIa-NH2 79 1771.01 886.8 1772.02 886.51 591.34 SP71 Ac-LTF$r8AYWAQL$AAIa-NH2 80 iso2 1771.01 887.09 1772.02 886.51 591.34 SP72 Ac-LTF$r8AYWAAL$AAMa-NH2 81 1731.94 867.17 1732.95 866.98 578.32 SP73 Ac-LTF$r8AYWAAL$AAMa-NH2 82 iso2 1731.94 867.37 1732.95 866.98 578.32 SP74 Ac-LTF$r8AYWAQL$AANlea-NH2 83 1771.01 887.08 1772.02 886.51 591.34 SP75 Ac-LTF$r8AYWAQL$AANlea-NH2 84 iso2 1771.01 887.08 1772.02 886.51 591.34 SP76 Ac-LTF$r8AYWAAL$AAIv-NH2 85 1742.02 872.37 1743.03 872.02 581.68 SP77 Ac-LTF$r8AYWAAL$AAIv-NH2 86 iso2 1742.02 872.74 1743.03 872.02 581.68 SP78 Ac-LTF$r8AYWAQL$AAMv-NH2 87 1817 910.02 1818.019 09.51 606.67 SP79 Ac-LTF$r8AYWAAL$AANlev-NH2 88 1742.02 872.37 1743.03 872.02 581.68 SP80 Ac-LTF$r8AYWAAL$AANlev-NH2 89 iso2 1742.02 872.28 1743.03 872.02 581.68 SP81 Ac-LTF$r8AYWAQL$AAIl-NH2 90 1813.05 907.81 1814.06 907.53 605.36 SP82 Ac-LTF$r8AYWAQL$AAIl-NH2 91 iso2 1813.05 907.81 1814.06 907.53 605.36 SP83 Ac-LTF$r8AYWAAL$AAMl-NH2 92 1773.99 887.37 1775 888 592.34 SP84 Ac-LTF$r8AYWAQL$AANlel-NH2 93 1813.05 907.61 1814.06 907.53 605.36 SP85 Ac-LTF$r8AYWAQL$AANlel-NH2 94 iso2 1813.05 907.71 1814.06 907.53 605.36 SP86 Ac-F$r8AYWEAL$AAMA-NH2 95 1575.82 789.02 1576.83 788.92 526.28 SP87 Ac-F$r8AYWEAL$AANleA-NH2 96 1557.86 780.14 1558.87 779.94 520.29 SP88 Ac-F$r8AYWEAL$AAIa-NH2 97 1557.86 780.33 1558.87 779.94 520.29 SP89 Ac-F$r8AYWEAL$AAMa-NH2 98 1575.82 789.3 1576.83 788.92 526.28 SP90 Ac-F$r8AYWEAL$AANlea-NH2 99 1557.86 779.4 1558.87 779.94 520.29 SP91 Ac-F$r8AYWEAL$AAIv-NH2 100 1585.89 794.29 1586.9 793.95 529.64 SP92 Ac-F$r8AYWEAL$AAMv-NH2 101 1603.85 803.08 1604.86 802.93 535.62 SP93 Ac-F$r8AYWEAL$AANlev-NH2 102 1585.89 793.46 1586.9 793.95 529.64 SP94 Ac-F$r8AYWEAL$AAIl-NH2 103 1599.91 800.49 1600.92 800.96 534.31 SP95 Ac-F$r8AYWEAL$AAMl-NH2 104 1617.86 809.44 1618.87 809.94 540.29 SP96 Ac-F$r8AYWEAL$AANlel-NH2 105 1599.91 801.7 1600.92 800.96 534.31 SP97 Ac-F$r8AYWEAL$AANlel-NH2 106 iso2 1599.91 801.42 1600.92 800.96 534.31 SP98 Ac-LTF$r8AY6clWAQL$SAA-NH2 107 1707.88 855.72 1708.89 854.95 570.3 SP99 Ac-LTF$r8AY6clWAQL$SAA-NH2 108 iso2 1707.88 855.35 1708.89 854.95 570.3 SP100 Ac-WTF$r8FYWSQL$AVAa-NH2 109 1922.01 962.21 1923.02 962.01 641.68 SP101 Ac-WTF$r8FYWSQL$AVAa-NH2 110 iso2 1922.01 962.49 1923.02 962.01 641.68 SP102 Ac-WTF$r8VYWSQL$AVA-NH2 111 1802.98 902.72 1803.99 902.5 602 SP103 Ac-WTF$r8VYWSQL$AVA-NH2 112 iso2 1802.98 903 1803.99 902.5 602 SP104 Ac-WTF$r8FYWSQL$SAAa-NH2 113 1909.98 956.47 1910.99 956 637.67 SP105 Ac-WTF$r8FYWSQL$SAAa-NH2 114 iso2 1909.98 956.47 1910.99 956 637.67 SP106 Ac-WTF$r8VYWSQL$AVAaa-NH2 115 1945.05 974.15 1946.06 973.53 649.36 SP107 Ac-WTF$r8VYWSQL$AVAaa-NH2 116 iso2 1945.05 973.78 1946.06 973.53 649.36 SP108 Ac-LTF$r8AYWAQL$AVG-NH2 117 1671.94 837.52 1672.95 836.98 558.32 SP109 Ac-LTF$r8AYWAQL$AVG-NH2 118 iso2 1671.94 837.21 1672.95 836.98 558.32 SP110 Ac-LTF$r8AYWAQL$AVQ-NH2 119 1742.98 872.74 1743.99 872.5 582 SP111 Ac-LTF$r8AYWAQL$AVQ-NH2 120 iso2 1742.98 872.74 1743.99 872.5 582 SP112 Ac-LTF$r8AYWAQL$SAa-NH2 121 1673.92 838.23 1674.93 837.97 558.98 SP113 Ac-LTF$r8AYWAQL$SAa-NH2 122 iso2 1673.92 838.32 1674.93 837.97 558.98 SP114 Ac-LTF$r8AYWAQhL$SAA-NH2 123 1687.93 844.37 1688.94 844.97 563.65 SP115 Ac-LTF$r8AYWAQhL$SAA-NH2 124 iso2 1687.93 844.81 1688.94 844.97 563.65 SP116 Ac-LTF$r8AYWEQLStSA$-NH2 125 1826 905.27 1827.01 914.01 609.67 SP117 Ac-LTF$r8AYWAQL$SLA-NH2 126 1715.97 858.48 1716.98 858.99 573 SP118 Ac-LTF$r8AYWAQL$SLA-NH2 127 iso2 1715.97 858.87 1716.98 858.99 573 SP119 Ac-LTF$r8AYWAQL$SWA-NH2 128 1788.96 895.21 1789.97 895.49 597.33 SP120 Ac-LTF$r8AYWAQL$SWA-NH2 129 iso2 1788.96 895.28 1789.97 895.49 597.33 SP121 Ac-LTF$r8AYWAQL$SVS-NH2 130 1717.94 859.84 1718.95 859.98 573.65 SP122 Ac-LTF$r8AYWAQL$SAS-NH2 131 1689.91 845.85 1690.92 845.96 564.31 SP123 Ac-LTF$r8AYWAQL$SVG-NH2 132 1687.93 844.81 1688.94 844.97 563.65 SP124 Ac-ETF$r8VYWAQL$SAa-NH2 133 1717.91 859.76 1718.92 859.96 573.64 SP125 Ac-ETF$r8VYWAQL$SAA-NH2 134 1717.91 859.84 1718.92 859.96 573.64 SP126 Ac-ETF$r8VYWAQL$SVA-NH2 135 1745.94 873.82 1746.95 873.98 582.99 SP127 Ac-ETF$r8VYWAQL$SLA-NH2 136 1759.96 880.85 1760.97 880.99 587.66 SP128 Ac-ETF$r8VYWAQL$SWA-NH2 137 1832.95 917.34 1833.96 917.48 611.99 SP129 Ac-ETF$r8KYWAQL$SWA-NH2 138 1861.98 931.92 1862.99 932 621.67 SP130 Ac-ETF$r8VYWAQL$SVS-NH2 139 1761.93 881.89 1762.94 881.97 588.32 SP131 Ac-ETF$r8VYWAQL$SAS-NH2 140 1733.9 867.83 1734.91 867.96 578.97 SP132 Ac-ETF$r8VYWAQL$SVG-NH2 141 1731.92 866.87 1732.93 866.97 578.31 SP133 Ac-LTF$r8VYWAQL$SSa-NH2 142 1717.94 859.47 1718.95 859.98 573.65 SP134 Ac-ETF$r8VYWAQL$SSa-NH2 143 1733.9 867.83 1734.91 867.96 578.97 SP135 Ac-LTF$r8VYWAQL$SNa-NH2 144 1744.96 873.38 1745.97 873.49 582.66 SP136 Ac-ETF$r8VYWAQL$SNa-NH2 145 1760.91 881.3 1761.92 881.46 587.98 SP137 Ac-LTF$r8VYWAQL$SAa-NH2 146 1701.95 851.84 1702.96 851.98 568.32 SP138 Ac-LTF$r8VYWAQL$SVA-NH2 147 1729.98 865.53 1730.99 866 577.67 SP139 Ac-LTF$r8VYWAQL$SVA-NH2 148 iso2 1729.98 865.9 1730.99 866 577.67 SP140 Ac-LTF$r8VYWAQL$SWA-NH2 149 1816.99 909.42 1818 909.5 606.67 SP141 Ac-LTF$r8VYWAQL$SVS-NH2 150 1745.98 873.9 1746.99 874 583 SP142 Ac-LTF$r8VYWAQL$SVS-NH2 151 iso2 1745.98 873.9 1746.99 874 583 SP143 Ac-LTF$r8VYWAQL$SAS-NH2 152 1717.94 859.84 1718.95 859.98 573.65 SP144 Ac-LTF$r8VYWAQL$SAS-NH2 153 iso2 1717.94 859.91 1718.95 859.98 573.65 SP145 Ac-LTF$r8VYWAQL$SVG-NH2 154 1715.97 858.87 1716.98 858.99 573 SP146 Ac-LTF$r8VYWAQL$SVG-NH2 155 iso2 1715.97 858.87 1716.98 858.99 573 SP147 Ac-LTF$r8EYWAQCha$SAA-NH2 156 1771.96 886.85 1772.97 886.99 591.66 SP148 Ac-LTF$r8EYWAQCha$SAA-NH2 157 iso2 1771.96 886.85 1772.97 886.99 591.66 SP149 Ac-LTF$r8EYWAQCpg$SAA-NH2 158 1743.92 872.86 1744.93 872.97 582.31 SP150 Ac-LTF$r8EYWAQCpg$SAA-NH2 159 iso2 1743.92 872.86 1744.93 872.97 582.31 SP151 Ac-LTF$r8EYWAQF$SAA-NH2 160 1765.91 883.44 1766.92 883.96 589.64 SP152 Ac-LTF$r8EYWAQF$SAA-NH2 161 iso2 1765.91 883.89 1766.92 883.96 589.64 SP153 Ac-LTF$r8EYWAQCba$SAA-NH2 162 1743.92 872.42 1744.93 872.97 582.31 SP154 Ac-LTF$r8EYWAQCba$SAA-NH2 163 iso2 1743.92 873.39 1744.93 872.97 582.31 SP155 Ac-LTF3C1$r8EYWAQL$SAA-NH2 164 1765.89 883.89 1766.9 883.95 589.64 SP156 Ac-LTF3C1$r8EYWAQL$SAA-NH2 165 iso2 1765.89 883.96 1766.9 883.95 589.64 SP157 Ac-LTF34F2$r8EYWAQL$SAA-NH2 166 1767.91 884.48 1768.92 884.96 590.31 SP158 Ac-LTF34F2$r8EYWAQL$SAA-NH2 167 iso2 1767.91 884.48 1768.92 884.96 590.31 SP159 Ac-LTF34F2$r8EYWAQhL$SAA-NH2 168 1781.92 891.44 1782.93 891.97 594.98 SP160 Ac-LTF34F2$r8EYWAQhL$SAA-NH2 169 iso2 1781.92 891.88 1782.93 891.97 594.98 SP161 Ac-ETF$r8EYWAQL$SAA-NH2 170 1747.88 874.34 1748.89 874.95 583.63 SP162 Ac-LTF$r8AYWVQL$SAA-NH2 171 1701.95 851.4 1702.96 851.98 568.32 SP163 Ac-LTF$r8AHWAQL$SAA-NH2 172 1647.91 824.83 1648.92 824.96 550.31 SP164 Ac-LTF$r8AEWAQL$SAA-NH2 173 1639.9 820.39 1640.91 820.96 547.64 SP165 Ac-LTF$r8ASWAQL$SAA-NH2 174 1597.89 799.38 1598.9 799.95 533.64 SP166 Ac-LTF$r8AEWAQL$SAA-NH2 175 iso2 1639.9 820.39 1640.91 820.96 547.64 SP167 Ac-LTF$r8ASWAQL$SAA-NH2 176 iso2 1597.89 800.31 1598.9 799.95 533.64 SP168 Ac-LTF$r8AF4coohWAQL$SAA-NH2 177 1701.91 851.4 1702.92 851.96 568.31 SP169 Ac-LTF$r8AF4coohWAQL$SAA-NH2 178 iso2 1701.91 851.4 1702.92 851.96 568.31 SP170 Ac-LTF$r8AHWAQL$AAIa-NH2 179 1745 874.13 1746.01 873.51 582.67 SP171 Ac-ITF$r8FYWAQL$AAIa-NH2 180 1847.04 923.92 1848.05 924.53 616.69 SP172 Ac-ITF$r8EHWAQL$AAIa-NH2 181 1803.01 903.17 1804.02 902.51 602.01 SP173 Ac-ITF$r8EHWAQL$AAIa-NH2 182 iso2 1803.01 903.17 1804.02 902.51 602.01 SP174 Ac-ETF$r8EHWAQL$AAIa-NH2 183 1818.97 910.76 1819.98 910.49 607.33 SP175 Ac-ETF$r8EHWAQL$AAIa-NH2 184 iso2 1818.97 910.85 1819.98 910.49 607.33 SP176 Ac-LTF$r8AHWVQL$AAIa-NH2 185 1773.03 888.09 1774.04 887.52 592.02 SP177 Ac-ITF$r8FYWVQL$AAIa-NH2 186 1875.07 939.16 1876.08 938.54 626.03 SP178 Ac-ITF$r8EYWVQL$AAIa-NH2 187 1857.04 929.83 1858.05 929.53 620.02 SP179 Ac-ITF$r8EHWVQL$AAIa-NH2 188 1831.04 916.86 1832.05 916.53 611.35 SP180 Ac-LTF$r8AEWAQL$AAIa-NH2 189 1736.99 869.87 1738 869.5 580 SP181 Ac-LTF$r8AF4coohWAQL$AAIa-NH2 190 1799 900.17 1800.01 900.51 600.67 SP182 Ac-LTF$r8AF4coohWAQL$AAIa-NH2 191 iso2 1799 900.24 1800.01 900.51 600.67 SP183 Ac-LTF$r8AHWAQL$AHFA-NH2 192 1845.01 923.89 1846.02 923.51 616.01 SP184 Ac-ITF$r8FYWAQL$AHFA-NH2 193 1947.05 975.05 1948.06 974.53 650.02 SP185 Ac-ITF$r8FYWAQL$AHFA-NH2 194 iso2 1947.05 976.07 1948.06 974.53 650.02 SP186 Ac-ITF$r8FHWAQL$AEFA-NH2 195 1913.02 958.12 1914.03 957.52 638.68 SP187 Ac-ITF$r8FHWAQL$AEFA-NH2 196 iso2 1913.02 957.86 1914.03 957.52 638.68 SP188 Ac-ITF$r8EHWAQL$AHFA-NH2 197 1903.01 952.94 1904.02 952.51 635.34 SP189 Ac-ITF$r8EHWAQL$AHFA-NH2 198 iso2 1903.01 953.87 1904.02 952.51 635.34 SP190 Ac-LTF$r8AHWVQL$AHFA-NH2 199 1873.04 937.86 1874.05 937.53 625.35 SP191 Ac-ITF$r8FYWVQL$AHFA-NH2 200 1975.08 988.83 1976.09 988.55 659.37 SP192 Ac-ITF$r8EYWVQL$AHFA-NH2 201 1957.05 979.35 1958.06 979.53 653.36 SP193 Ac-ITF$r8EHWVQL$AHFA-NH2 202 1931.05 967 1932.06 966.53 644.69 SP194 Ac-ITF$r8EHWVQL$AHFA-NH2 203 iso2 1931.05 967.93 1932.06 966.53 644.69 SP195 Ac-ETF$r8EYWAAL$SAA-NH2 204 1690.86 845.85 1691.87 846.44 564.63 SP196 Ac-LTF$r8AYWVAL$SAA-NH2 205 1644.93 824.08 1645.94 823.47 549.32 SP197 Ac-LTF$r8AHWAAL$SAA-NH2 206 1590.89 796.88 1591.9 796.45 531.3 SP198 Ac-LTF$r8AEWAAL$SAA-NH2 207 1582.88 791.9 1583.89 792.45 528.63 SP199 Ac-LTF$r8AEWAAL$SAA-NH2 208 iso2 1582.88 791.9 1583.89 792.45 528.63 SP200 Ac-LTF$r8ASWAAL$SAA-NH2 209 1540.87 770.74 1541.88 771.44 514.63 SP201 Ac-LTF$r8ASWAAL$SAA-NH2 210 iso2 1540.87 770.88 1541.88 771.44 514.63 SP202 Ac-LTF$r8AYWAAL$AAIa-NH2 211 1713.99 857.39 1715 858 572.34 SP203 Ac-LTF$r8AYWAAL$AAIa-NH2 212 iso2 1713.99 857.84 1715 858 572.34 SP204 Ac-LTF$r8AYWAAL$AHFA-NH2 213 1813.99 907.86 1815 908 605.67 SP205 Ac-LTF$r8EHWAQL$AHIa-NH2 214 1869.03 936.1 1870.04 935.52 624.02 SP206 Ac-LTF$r8EHWAQL$AHIa-NH2 215 iso2 1869.03 937.03 1870.04 935.52 624.02 SP207 Ac-LTF$r8AHWAQL$AHIa-NH2 216 1811.03 906.87 1812.04 906.52 604.68 SP208 Ac-LTF$r8EYWAQL$AHIa-NH2 217 1895.04 949.15 1896.05 948.53 632.69 SP209 Ac-LTF$r8AYWAQL$AAFa-NH2 218 1804.99 903.2 1806 903.5 602.67 SP210 Ac-LTF$r8AYWAQL$AAFa-NH2 219 iso2 1804.99 903.28 1806 903.5 602.67 SP211 Ac-LTF$r8AYWAQL$AAWa-NH2 220 1844 922.81 1845.01 923.01 615.67 SP212 Ac-LTF$r8AYWAQL$AAVa-NH2 221 1756.99 878.86 1758 879.5 586.67 SP213 Ac-LTF$r8AYWAQL$AAVa-NH2 222 iso2 1756.99 879.3 1758 879.5 586.67 SP214 Ac-LTF$r8AYWAQL$AALa-NH2 223 1771.01 886.26 1772.02 886.51 591.34 SP215 Ac-LTF$r8AYWAQL$AALa-NH2 224 iso2 1771.01 886.33 1772.02 886.51 591.34 SP216 Ac-LTF$r8EYWAQL$AAIa-NH2 225 1829.01 914.89 1830.02 915.51 610.68 SP217 Ac-LTF$r8EYWAQL$AAIa-NH2 226 iso2 1829.01 915.34 1830.02 915.51 610.68 SP218 Ac-LTF$r8EYWAQL$AAFa-NH2 227 1863 932.87 1864.01 932.51 622.01 SP219 Ac-LTF$r8EYWAQL$AAFa-NH2 228 iso2 1863 932.87 1864.01 932.51 622.01 SP220 Ac-LTF$r8EYWAQL$AAVa-NH2 229 1815 908.23 1816.01 908.51 606.01 SP221 Ac-LTF$r8EYWAQL$AAVa-NH2 230 iso2 1815 908.31 1816.01 908.51 606.01 SP222 Ac-LTF$r8EHWAQL$AAIa-NH2 231 1803.01 903.17 1804.02 902.51 602.01 SP223 Ac-LTF$r8EHWAQL$AAIa-NH2 232 iso2 1803.01 902.8 1804.02 902.51 602.01 SP224 Ac-LTF$r8EHWAQL$AAWa-NH2 233 1876 939.34 1877.01 939.01 626.34 SP225 Ac-LTF$r8EHWAQL$AAWa-NH2 234 iso2 1876 939.62 1877.01 939.01 626.34 SP226 Ac-LTF$r8EHWAQL$AALa-NH2 235 1803.01 902.8 1804.02 902.51 602.01 SP227 Ac-LTF$r8EHWAQL$AALa-NH2 236 iso2 1803.01 902.9 1804.02 902.51 602.01 SP228 Ac-ETF$r8EHWVQL$AALa-NH2 237 1847 924.82 1848.01 924.51 616.67 SP229 Ac-LTF$r8AYWAQL$AAAa-NH2 238 1728.96 865.89 1729.97 865.49 577.33 SP230 Ac-LTF$r8AYWAQL$AAAa-NH2 239 iso2 1728.96 865.89 1729.97 865.49 577.33 SP231 Ac-LTF$r8AYWAQL$AAAibA-NH2 240 1742.98 872.83 1743.99 872.5 582 SP232 Ac-LTF$r8AYWAQL$AAAibA-NH2 241 iso2 1742.98 872.92 1743.99 872.5 582 SP233 Ac-LTF$r8AYWAQL$AAAAa-NH2 242 1800 901.42 1801.01 901.01 601.01 SP234 Ac-LTF$r5AYWAQL$s8AAIa-NH2 243 1771.01 887.17 1772.02 886.51 591.34 SP235 Ac-LTF$r5AYWAQL$s8SAA-NH2 244 1673.92 838.33 1674.93 837.97 558.98 SP236 Ac-LTF$r8AYWAQCba$AANleA-NH2 245 1783.01 892.64 1784.02 892.51 595.34 SP237 Ac-ETF$r8AYWAQCba$AANleA-NH2 246 1798.97 900.59 1799.98 900.49 600.66 SP238 Ac-LTF$r8EYWAQCba$AANleA-NH2 247 1841.01 922.05 1842.02 921.51 614.68 SP239 Ac-LTF$r8AYWAQCba$AWNleA-NH2 248 1898.05 950.46 1899.06 950.03 633.69 SP240 Ac-ETF$r8AYWAQCba$AWNleA-NH2 249 1914.01 958.11 1915.02 958.01 639.01 SP241 Ac-LTF$r8EYWAQCba$AWNleA-NH2 250 1956.06 950.62 1957.07 979.04 653.03 SP242 Ac-LTF$r8EYWAQCba$SAFA-NH2 251 1890.99 946.55 1892 946.5 631.34 SP243 Ac-LTF34F2$r8EYWAQCba$SANleA-NH2 252 1892.99 947.57 1894 947.5 632 SP244 Ac-LTF$r8EF4coohWAQCba$SANleA-NH2 253 1885 943.59 1886.019 43.51 629.34 SP245 Ac-LTF$r8EYWSQCba$SANleA-NH2 254 1873 937.58 1874.019 37.51 625.34 SP246 Ac-LTF$r8EYWWQCba$SANleA-NH2 255 1972.05 987.61 1973.06 987.03 658.36 SP247 Ac-LTF$r8EYWAQCba$AAIa-NH2 256 1841.01 922.05 1842.02 921.51 614.68 SP248 Ac-LTF34F2$r8EYWAQCba$AAIa-NH2 257 1876.99 939.99 1878 939.5 626.67 SP249 Ac-LTF$r8EF4coohWAQCba$AAIa-NH2 258 1869.01 935.64 1870.02 935.51 624.01 SP250 Pam-ETF$r8EYWAQCba$SAA-NH2 259 1956.1 979.57 1957.11 979.06 653.04 SP251 Ac-LThF$r8EFWAQCba$SAA-NH2 260 1741.94 872.11 1742.95 871.98 581.65 SP252 Ac-LTA$r8EYWAQCba$SAA-NH2 261 1667.89 835.4 1668.9 834.95 556.97 SP253 Ac-LTF$r8EYAAQCba$SAA-NH2 262 1628.88 815.61 1629.89 815.45 543.97 SP254 Ac-LTF$r8EY2NalAQCba$SAA-NH2 263 1754.93 879.04 1755.94 878.47 585.98 SP255 Ac-LTF$r8AYWAQCba$SAA-NH2 264 1685.92 844.71 1686.93 843.97 562.98 SP256 Ac-LTF$r8EYWAQCba$SAF-NH2 265 1819.96 911.41 1820.97 910.99 607.66 SP257 Ac-LTF$r8EYWAQCba$SAFa-NH2 266 1890.99 947.41 1892 946.5 631.34 SP258 Ac-LTF$r8AYWAQCba$SAF-NH2 267 1761.95 882.73 1762.96 881.98 588.32 SP259 Ac-LTF34F2Sr8AYWAQCba$SAF-NH2 268 1797.93 900.87 1798.94 899.97 600.32 SP260 Ac-LTF$r8AF4coohWAQCba$SAF-NH2 269 1789.94 896.43 1790.95 895.98 597.65 SP261 Ac-LTF$r8EY6c1WAQCba$SAF-NH2 270 1853.92 929.27 1854.93 927.97 618.98 SP262 Ac-LTF$r8AYWSQCba$SAF-NH2 271 1777.94 890.87 1778.95 889.98 593.65 SP263 Ac-LTF$r8AYWWQCba$SAF-NH2 272 1876.99 939.91 1878 939.5 626.67 SP264 Ac-LTF$r8AYWAQCba$AAIa-NH2 273 1783.01 893.19 1784.02 892.51 595.34 SP265 Ac-LTF34F2$r8AYWAQCba$AAIa-NH2 274 1818.99 911.23 1820 910.5 607.34 SP266 Ac-LTF$r8AY6clWAQCba$AAIa-NH2 275 1816.97 909.84 1817.98 909.49 606.66 SP267 Ac-LTF$r8AF4coohWAQCba$AAIa-NH2 276 1811 906.88 1812.01 906.51 604.67 SP268 Ac-LTF$r8EYWAQCba$AAFa-NH2 277 1875 938.6 1876.01 938.51 626.01 SP269 Ac-LTF$r8EYWAQCba$AAFa-NH2 278 iso2 1875 938.6 1876.01 938.51 626.01 SP270 Ac-ETF$r8AYWAQCba$AWNlea-NH2 279 1914.01 958.42 1915.02 958.01 639.01 SP271 Ac-LTF$r8EYWAQCba$AWNlea-NH2 280 1956.06 979.42 1957.07 979.04 653.03 SP272 Ac-ETF$r8EYWAQCba$AWNlea-NH2 281 1972.01 987.06 1973.02 987.01 658.34 SP273 Ac-ETF$r8EYWAQCba$AWNlea-NH2 282 iso2 1972.01 987.06 1973.02 987.01 658.34 SP274 Ac-LTF$r8AYWAQCba$SAFa-NH2 283 1832.99 917.89 1834 917.5 612 SP275 Ac-LTF$r8AYWAQCba$SAFa-NH2 284 iso2 1832.99 918.07 1834 917.5 612 SP276 Ac-ETF$r8AYWAQL$AWNlea-NH2 285 1902.01 952.22 1903.02 952.01 635.01 SP277 Ac-LTF$r8EYWAQL$AWNlea-NH2 286 1944.06 973.5 1945.07 973.04 649.03 SP278 Ac-ETF$r8EYWAQL$AWNlea-NH2 287 1960.01 981.46 1961.02 981.01 654.34 SP279 Dmaac-LTF$r8EYWAQhL$SAA-NH2 288 1788.98 896.06 1789.99 895.5 597.33 SP280 Hexac-LTF$r8EYWAQhL$SAA-NH2 289 1802 902.9 1803.019 02.01 601.67 SP281 Napac-LTF$r8EYWAQhL$SAA-NH2 290 1871.99 937.58 1873 937 625 SP282 Decac-LTF$r8EYWAQhL$SAA-NH2 291 1858.06 930.55 1859.07 930.04 620.36 SP283 Admac-LTF$r8EYWAQhL$SAA-NH2 292 1866.03 934.07 1867.04 934.02 623.02 SP284 Tmac-LTF$r8EYWAQhL$SAA-NH2 293 1787.99 895.41 1789 895 597 SP285 Pam-LTF$r8EYWAQhL$SAA-NH2 294 1942.16 972.08 1943.17 972.09 648.39 SP286 Ac-LTF$r8AYWAQCba$AANleA-NH2 295 iso2 1783.01 892.64 1784.02 892.51 595.34 SP287 Ac-LTF34F2$r8EYWAQCba$AAIa-NH2 296 iso2 1876.99 939.62 1878 939.5 626.67 SP288 Ac-LTF34F2$r8EYWAQCba$SAA-NH2 297 1779.91 892.07 1780.92 890.96 594.31 SP289 Ac-LTF34F2$r8EYWAQCba$SAA-NH2 298 iso2 1779.91 891.61 1780.92 890.96 594.31 SP290 Ac-LTF$r8EF4coohWAQCba$SAA-NH2 299 1771.92 887.54 1772.93 886.97 591.65 SP291 Ac-LTF$r8EF4coohWAQCba$SAA-NH2 300 iso2 1771.92 887.63 1772.93 886.97 591.65 SP292 Ac-LTF$r8EYWSQCba$SAA-NH2 301 1759.92 881.9 1760.93 880.97 587.65 SP293 Ac-LTF$r8EYWSQCba$SAA-NH2 302 iso2 1759.92 881.9 1760.93 880.97 587.65 SP294 Ac-LTF$r8EYWAQhL$SAA-NH2 303 1745.94 875.05 1746.95 873.98 582.99 SP295 Ac-LTF$r8AYWAQhL$SAF-NH2 304 1763.97 884.02 1764.98 882.99 589 SP296 Ac-LTF$r8AYWAQhL$SAF-NH2 305 iso2 1763.97 883.56 1764.98 882.99 589 SP297 Ac-LTF34F2$r8AYWAQhL$SAA-NH2 306 1723.92 863.67 1724.93 862.97 575.65 SP298 Ac-LTF34F2$r8AYWAQhL$SAA-NH2 307 iso2 1723.92 864.04 1724.93 862.97 575.65 SP299 Ac-LTF$r8AF4coohWAQhL$SAA-NH2 308 1715.93 859.44 1716.94 858.97 572.98 SP300 Ac-LTF$r8AF4coohWAQhL$SAA-NH2 309 iso2 1715.93 859.6 1716.94 858.97 572.98 SP301 Ac-LTF$r8AYWSQhL$SAA-NH2 310 1703.93 853.96 1704.94 852.97 568.98 SP302 Ac-LTF$r8AYWSQhL$SAA-NH2 311 iso2 1703.93 853.59 1704.94 852.97 568.98 SP303 Ac-LTF$r8EYWAQL$AANleA-NH2 312 1829.01 915.45 1830.02 915.51 610.68 SP304 Ac-LTF34F2$r8AYWAQL$AANleA-NH2 313 1806.99 904.58 1808 904.5 603.34 SP305 Ac-LTF$r8AF4coohWAQL$AANleA-NH2 314 1799 901.6 1800.01 900.51 600.67 SP306 Ac-LTF$r8AYWSQL$AANleA-NH2 315 1787 894.75 1788.01 894.51 596.67 SP307 Ac-LTF34F2$r8AYWAQhL$AANleA-NH2 316 1821 911.79 1822.01 911.51 608.01 SP308 Ac-LTF34F2$r8AYWAQhL$AANleA-NH2 317 iso2 1821 912.61 1822.01 911.51 608.01 SP309 Ac-LTF$r8AF4coohWAQhL$AANleA-NH2 318 1813.02 907.95 1814.03 907.52 605.35 SP310 Ac-LTF$r8AF4coohWAQhL$AANleA-NH2 319 iso2 1813.02 908.54 1814.03 907.52 605.35 SP311 Ac-LTF$r8AYWSQhL$AANleA-NH2 320 1801.02 901.84 1802.03 901.52 601.35 SP312 Ac-LTF$r8AYWSQhL$AANleA-NH2 321 iso2 1801.02 902.62 1802.03 901.52 601.35 SP313 Ac-LTF$r8AYWAQhL$AAAAa-NH2 322 1814.01 908.63 1815.02 908.01 605.68 SP314 Ac-LTF$r8AYWAQhL$AAAAa-NH2 323 iso2 1814.01 908.34 1815.02 908.01 605.68 SP315 Ac-LTF$r8AYWAQL$AAAAAa-NH2 324 1871.04 936.94 1872.05 936.53 624.69 SP316 Ac-LTF$r8AYWAQL$AAAAAAa-NH2 325 iso2 1942.07 972.5 1943.08 972.04 648.37 SP317 Ac-LTF$r8AYWAQL$AAAAAAa-NH2 326 iso1 1942.07 972.5 1943.08 972.04 648.37 SP318 Ac-LTF$r8EYWAQhL$AANleA-NH2 327 1843.03 922.54 1844.04 922.52 615.35 SP319 Ac-AATF$r8AYWAQL$AANleA-NH2 328 1800 901.39 1801.01 901.01 601.01 SP320 Ac-LTF$r8AYWAQL$AANleAA-NH2 329 1842.04 922.45 1843.05 922.03 615.02 SP321 Ac-ALTF$r8AYWAQL$AANleAA-NH2 330 1913.08 957.94 1914.09 957.55 638.7 SP322 Ac-LTF$r8AYWAQCba$AANleAA-NH2 331 1854.04 928.43 1855.05 928.03 619.02 SP323 Ac-LTF$r8AYWAQhL$AANleAA-NH2 332 1856.06 929.4 1857.07 929.04 619.69 SP324 Ac-LTF$r8EYWAQCba$SAAA-NH2 333 1814.96 909.37 1815.97 908.49 605.99 SP325 Ac-LTF$r8EYWAQCba$SAAA-NH2 334 iso2 1814.96 909.37 1815.97 908.49 605.99 SP326 Ac-LTF$r8EYWAQCba$SAAAA-NH2 335 1886 944.61 1887.01 944.01 629.67 SP327 Ac-LTF$r8EYWAQCba$SAAAA-NH2 336 iso2 1886 944.61 1887.01 944.01 629.67 SP328 Ac-ALTF$r8EYWAQCba$SAA-NH2 337 1814.96 909.09 1815.97 908.49 605.99 SP329 Ac-ALTF$r8EYWAQCba$SAAA-NH2 338 1886 944.61 1887.01 944.01 629.67 SP330 Ac-ALTF$r8EYWAQCba$SAA-NH2 339 iso2 1814.96 909.09 1815.97 908.49 605.99 SP331 Ac-LTF$r8EYWAQL$AAAAAa-NH2 340 iso2 1929.04 966.08 1930.05 965.53 644.02 SP332 Ac-LTF$r8EY6clWAQCba$SAA-NH2 341 1777.89 890.78 1778.9 889.95 593.64 SP333 Ac-LTF$r8EF4cooh6c1WAQCba$SANleA- 342 1918.96 961.27 1919.97 960.49 640.66 NH2 SP334 Ac-LTF$r8EF4cooh6c1WAQCba$SANleA- 343 iso2 1918.96 961.27 1919.97 960.49 640.66 NH2 SP335 Ac-LTF$r8EF4cooh6clWAQCba$AAIa-NH2 344 1902.97 953.03 1903.98 952.49 635.33 SP336 Ac-LTF$r8EF4cooh6clWAQCba$AAIa-NH2 345 iso2 1902.97 953.13 1903.98 952.49 635.33 SP337 Ac-LTF$r8AY6clWAQL$AAAAAa-NH2 346 1905 954.61 1906.01 953.51 636.01 SP338 Ac-LTF$r8AY6clWAQL$AAAAAa-NH2 347 iso2 1905 954.9 1906.01 953.51 636.01 SP339 Ac-F$r8AY6clWEAL$AAAAAAa-NH2 348 1762.89 883.01 1763.9 882.45 588.64 SP340 Ac-ETF$r8EYWAQL$AAAAAa-NH2 349 1945 974.31 1946.01 973.51 649.34 SP341 Ac-ETF$r8EYWAQL$AAAAAa-NH2 350 iso2 1945 974.49 1946.01 973.51 649.34 SP342 Ac-LTF$r8EYWAQL$AAAAAAa-NH2 351 2000.08 1001.6 2001.09 1001.05 667.7 SP343 Ac-LTF$r8EYWAQL$AAAAAAa-NH2 352 iso2 2000.08 1001.6 2001.09 1001.05 667.7 SP344 Ac-LTF$r8AYWAQL$AANleAAa-NH2 353 1913.08 958.58 1914.09 957.55 638.7 SP345 Ac-LTF$r8AYWAQL$AANleAAa-NH2 354 iso2 1913.08 958.58 1914.09 957.55 638.7 SP346 Ac-LTF$r8EYWAQCba$AAAAAa-NH2 355 1941.04 972.55 1942.05 971.53 648.02 SP347 Ac-LTF$r8EYWAQCba$AAAAAa-NH2 356 iso2 1941.04 972.55 1942.05 971.53 648.02 SP348 Ac-LTF$r8EF4coohWAQCba$AAAAAa-NH2 357 1969.04 986.33 1970.05 985.53 657.35 SP349 Ac-LTF$r8EF4coohWAQCba$AAAAAa-NH2 358 iso2 1969.04 986.06 1970.05 985.53 657.35 SP350 Ac-LTF$r8EYWSQCba$AAAAAa-NH2 359 1957.04 980.04 1958.05 979.53 653.35 SP351 Ac-LTF$r8EYWSQCba$AAAAAa-NH2 360 iso2 1957.04 980.04 1958.05 979.53 653.35 SP352 Ac-LTF$r8EYWAQCba$SAAa-NH2 361 1814.96 909 1815.97 908.49 605.99 SP353 Ac-LTF$r8EYWAQCba$SAAa-NH2 362 iso2 1814.96 909 1815.97 908.49 605.99 SP354 Ac-ALTF$r8EYWAQCba$SAAa-NH2 363 1886 944.52 1887.01 944.01 629.67 SP355 Ac-ALTF$r8EYWAQCba$SAAa-NH2 364 iso2 1886 944.98 1887.01 944.01 629.67 SP356 Ac-ALTF$r8EYWAQCba$SAAAa-NH2 365 1957.04 980.04 1958.05 979.53 653.35 SP357 Ac-ALTF$r8EYWAQCba$SAAAa-NH2 366 iso2 1957.04 980.04 1958.05 979.53 653.35 SP358 Ac-AALTF$r8EYWAQCba$SAAAa-NH2 367 2028.07 1016.1 2029.08 1015.04 677.03 SP359 Ac-AALTF$r8EYWAQCba$SAAAa-NH2 368 iso2 2028.07 1015.57 2029.08 1015.04 677.03 SP360 Ac-RTF$r8EYWAQCba$SAA-NH2 369 1786.94 895.03 1787.95 894.48 596.65 SP361 Ac-LRF$r8EYWAQCba$SAA-NH2 370 1798.98 901.51 1799.99 900.5 600.67 SP362 Ac-LTF$r8EYWRQCba$SAA-NH2 371 1828.99 916.4 1830 915.5 610.67 SP363 Ac-LTF$r8EYWARCba$SAA-NH2 372 1771.97 887.63 1772.98 886.99 591.66 SP364 Ac-LTF$r8EYWAQCba$RAA-NH2 373 1812.99 908.08 1814 907.5 605.34 SP365 Ac-LTF$r8EYWAQCba$SRA-NH2 374 1828.99 916.12 1830 915.5 610.67 SP366 Ac-LTF$r8EYWAQCba$SAR-NH2 375 1828.99 916.12 1830 915.5 610.67 SP367 5-FAM-BaLTF$r8EYWAQCba$SAA-NH2 376 2131 1067.09 2132.01 1066.51 711.34 SP368 5-FAM-BaLTF$r8AYWAQL$AANleA-NH2 377 2158.08 1080.6 2159.09 1080.05 720.37 SP369 Ac-LAF$r8EYWAQL$AANleA-NH2 378 1799 901.05 1800.01 900.51 600.67 SP370 Ac-ATF$r8EYWAQL$AANleA-NH2 379 1786.97 895.03 1787.98 894.49 596.66 SP371 Ac-AAF$r8EYWAQL$AANleA-NH2 380 1756.96 880.05 1757.97 879.49 586.66 SP372 Ac-AAAF$r8EYWAQL$AANleA-NH2 381 1827.99 915.57 1829 915 610.34 SP373 Ac-AAAAF$r8EYWAQL$AANleA-NH2 382 1899.03 951.09 1900.04 950.52 634.02 SP374 Ac-AATF$r8EYWAQL$AANleA-NH2 383 1858 930.92 1859.01 930.01 620.34 SP375 Ac-AALTF$r8EYWAQL$AANleA-NH2 384 1971.09 987.17 1972.1 986.55 658.04 SP376 Ac-AAALTF$r8EYWAQL$AANleA-NH2 385 2042.12 1023.15 2043.13 1022.07 681.71 SP377 Ac-LTF$r8EYWAQL$AANleAA-NH2 386 1900.05 952.02 1901.06 951.03 634.36 SP378 Ac-ALTF$r8EYWAQL$AANleAA-NH2 387 1971.09 987.63 1972.1 986.55 658.04 SP379 Ac-AALTF$r8EYWAQL$AANleAA-NH2 388 2042.12 1022.69 2043.13 1022.07 681.71 SP380 Ac-LTF$r8EYWAQCba$AANleAA-NH2 389 1912.05 958.03 1913.06 957.03 638.36 SP381 Ac-LTF$r8EYWAQhL$AANleAA-NH2 390 1914.07 958.68 1915.08 958.04 639.03 SP382 Ac-ALTF$r8EYWAQhL$AANleAA-NH2 391 1985.1 994.1 1986.11 993.56 662.71 SP383 Ac-LTF$r8ANmYWAQL$AANleA-NH2 392 1785.02 894.11 1786.03 893.52 596.01 SP384 Ac-LTF$r8ANmYWAQL$AANleA-NH2 393 iso2 1785.02 894.11 1786.03 893.52 596.01 SP385 Ac-LTF$r8AYNmWAQL$AANleA-NH2 394 1785.02 894.11 1786.03 893.52 596.01 SP386 Ac-LTF$r8AYNmWAQL$AANleA-NH2 395 iso2 1785.02 894.11 1786.03 893.52 596.01 SP387 Ac-LTF$r8AYAmwAQL$AANleA-NH2 396 1785.02 894.01 1786.03 893.52 596.01 SP388 Ac-LTF$r8AYAmwAQL$AANleA-NH2 397 iso2 1785.02 894.01 1786.03 893.52 596.01 SP389 Ac-LTF$r8AYWAibQL$AANleA-NH2 398 1785.02 894.01 1786.03 893.52 596.01 SP390 Ac-LTF$r8AYWAibQL$AANleA-NH2 399 iso2 1785.02 894.01 1786.03 893.52 596.01 SP391 Ac-LTF$r8AYWAQL$AAibNleA-NH2 400 1785.02 894.38 1786.03 893.52 596.01 SP392 Ac-LTF$r8AYWAQL$AAibNleA-NH2 401 iso2 1785.02 894.38 1786.03 893.52 596.01 SP393 Ac-LTF$r8AYWAQL$AaNleA-NH2 402 1771.01 887.54 1772.02 886.51 591.34 SP394 Ac-LTF$r8AYWAQL$AaNleA-NH2 403 iso2 1771.01 887.54 1772.02 886.51 591.34 SP395 Ac-LTF$r8AYWAQL$ASarNleA-NH2 404 1771.01 887.35 1772.02 886.51 591.34 SP396 Ac-LTF$r8AYWAQL$ASarNleA-NH2 405 iso2 1771.01 887.35 1772.02 886.51 591.34 SP397 Ac-LTF$r8AYWAQL$AANleAib-NH2 406 1785.02 894.75 1786.03 893.52 596.01 SP398 Ac-LTF$r8AYWAQL$AANleAib-NH2 407 iso2 1785.02 894.75 1786.03 893.52 596.01 SP399 Ac-LTF$r8AYWAQL$AANleNmA-NH2 408 1785.02 894.6 1786.03 893.52 596.01 SP400 Ac-LTF$r8AYWAQL$AANleNmA-NH2 409 iso2 1785.02 894.6 1786.03 893.52 596.01 SP401 Ac-LTF$r8AYWAQL$AANleSar-NH2 410 1771.01 886.98 1772.02 886.51 591.34 SP402 Ac-LTF$r8AYWAQL$AANleSar-NH2 411 iso2 1771.01 886.98 1772.02 886.51 591.34 SP403 Ac-LTF$r8AYWAQL$AANleAAib-NH2 412 1856.06 1857.07 929.04 619.69 SP404 Ac-LTF$r8AYWAQL$AANleAAib-NH2 413 iso2 1856.06 1857.07 929.04 619.69 SP405 Ac-LTF$r8AYWAQL$AANleANmA-NH2 414 1856.06 930.37 1857.07 929.04 619.69 SP406 Ac-LTF$r8AYWAQL$AANleANmA-NH2 415 iso2 1856.06 930.37 1857.07 929.04 619.69 SP407 Ac-LTF$r8AYWAQL$AANleAa-NH2 416 1842.04 922.69 1843.05 922.03 615.02 SP408 Ac-LTF$r8AYWAQL$AANleAa-NH2 417 iso2 1842.04 922.69 1843.05 922.03 615.02 SP409 Ac-LTF$r8AYWAQL$AANleASar-NH2 418 1842.04 922.6 1843.05 922.03 615.02 SP410 Ac-LTF$r8AYWAQL$AANleASar-NH2 419 iso2 1842.04 922.6 1843.05 922.03 615.02 SP411 Ac-LTF$/r8AYWAQL$/AANleA-NH2 420 1799.04 901.14 1800.05 900.53 600.69 SP412 Ac-LTFAibAYWAQLAibAANleA-NH2 421 1648.9 826.02 1649.91 825.46 550.64 SP413 Ac-LTF$r8Cou4YWAQL$AANleA-NH2 422 1975.05 989.11 1976.06 988.53 659.36 SP414 Ac-LTF$r8Cou4YWAQL$AANleA-NH2 423 iso2 1975.05 989.11 1976.06 988.53 659.36 SP415 Ac-LTF$r8AYWCou4QL$AANleA-NH2 424 1975.05 989.11 1976.06 988.53 659.36 SP416 Ac-LTF$r8AYWAQL$Cou4ANleA-NH2 425 1975.05 989.57 1976.06 988.53 659.36 SP417 Ac-LTF$r8AYWAQL$Cou4ANleA-NH2 426 iso2 1975.05 989.57 1976.06 988.53 659.36 SP418 Ac-LTF$r8AYWAQL$ACou4NleA-NH2 427 1975.05 989.57 1976.06 988.53 659.36 SP419 Ac-LTF$r8AYWAQL$ACou4NleA-NH2 428 iso2 1975.05 989.57 1976.06 988.53 659.36 SP420 Ac-LTF$r8AYWAQL$AANleA-OH 429 1771.99 887.63 1773 887 591.67 SP421 Ac-LTF$r8AYWAQL$AANleA-OH 430 iso2 1771.99 887.63 1773 887 591.67 SP422 Ac-LTF$r8AYWAQL$AANleA-NHnPr 431 1813.05 908.08 1814.06 907.53 605.36 SP423 Ac-LTF$r8AYWAQL$AANleA-NHnPr 432 iso2 1813.05 908.08 1814.06 907.53 605.36 SP424 Ac-LTF$r8AYWAQL$AANleA-NHnBu33Me 433 1855.1 929.17 1856.11 928.56 619.37 SP425 Ac-LTF$r8AYWAQL$AANleA-NHnBu33Me 434 iso2 1855.1 929.17 1856.11 928.56 619.37 SP426 Ac-LTF$r8AYWAQL$AANleA-NHHex 435 1855.1 929.17 1856.11 928.56 619.37 SP427 Ac-LTF$r8AYWAQL$AANleA-NHHex 436 iso2 1855.1 929.17 1856.11 928.56 619.37 SP428 Ac-LTA$r8AYWAQL$AANleA-NH2 437 1694.98 849.33 1695.99 848.5 566 SP429 Ac-LThL$r8AYWAQL$AANleA-NH2 438 1751.04 877.09 1752.05 876.53 584.69 SP430 Ac-LTF$r8AYAAQL$AANleA-NH2 439 1655.97 829.54 1656.98 828.99 553 SP431 Ac-LTF$r8AY2NalAQL$AANleA-NH2 440 1782.01 892.63 1783.02 892.01 595.01 SP432 Ac-LTF$r8EYWCou4QCba$SAA-NH2 441 1947.97 975.8 1948.98 974.99 650.33 SP433 Ac-LTF$r8EYWCou7QCba$SAA-NH2 442 16.03 974.9 17.04 9.02 6.35 SP434 Ac-LTF%r8EYWAQCba%SAA-NH2 443 1745.94 874.8 1746.95 873.98 582.99 SP435 Dmaac-LTF$r8EYWAQCba$SAA-NH2 444 1786.97 894.8 1787.98 894.49 596.66 SP436 Dmaac-LTF$r8AYWAQL$AAAAAa-NH2 445 1914.08 958.2 1915.09 958.05 639.03 SP437 Dmaac-LTF$r8AYWAQL$AAAAAa-NH2 446 iso2 1914.08 958.2 1915.09 958.05 639.03 SP438 Dmaac-LTF$r8EYWAQL$AAAAAa-NH2 447 1972.08 987.3 1973.09 987.05 658.37 SP439 Dmaac-LTF$r8EYWAQL$AAAAAa-NH2 448 iso2 1972.08 987.3 1973.09 987.05 658.37 SP440 Dmaac-LTF$r8EF4coohWAQCba$AAIa-NH2 449 1912.05 957.4 1913.06 957.03 638.36 SP441 Dmaac-LTF$r8EF4coohWAQCba$AAIa-NH2 450 iso2 1912.05 957.4 1913.06 957.03 638.36 SP442 Dmaac-LTF$r8AYWAQL$AANleA-NH2 451 1814.05 908.3 1815.06 908.03 605.69 SP443 Dmaac-LTF$r8AYWAQL$AANleA-NH2 452 iso2 1814.05 908.3 1815.06 908.03 605.69 SP444 Ac-LTF%r8AYWAQL%AANleA-NH2 453 1773.02 888.37 1774.03 887.52 592.01 SP445 Ac-LTF%r8EYWAQL%AAAAAa-NH2 454 1931.06 966.4 1932.07 966.54 644.69 SP446 Cou6BaLTF$r8EYWAQhL$SAA-NH2 455 2018.05 1009.9 2019.06 1010.03 673.69 SP447 Cou8BaLTF$r8EYWAQhL$SAA-NH2 456 1962.96 982.34 1963.97 982.49 655.32 SP448 Ac-LTF4I$r8EYWAQL$AAAAAa-NH2 457 2054.93 1028.68 2055.94 1028.47 685.98 SP449 Ac-LTF$r8EYWAQL$AAAAAa-NH2 458 1929.04 966.17 1930.05 965.53 644.02 SP550 Ac-LTF$r8EYWAQL$AAAAAa-OH 459 1930.02 966.54 1931.03 966.02 644.35 SP551 Ac-LTF$r8EYWAQL$AAAAAa-OH 460 iso2 1930.02 965.89 1931.03 966.02 644.35 SP552 Ac-LTF$r8EYWAEL$AAAAAa-NH2 461 1930.02 966.82 1931.03 966.02 644.35 SP553 Ac-LTF$r8EYWAEL$AAAAAa-NH2 462 iso2 1930.02 966.91 1931.03 966.02 644.35 SP554 Ac-LTF$r8EYWAEL$AAAAAa-OH 463 1931.01 967.28 1932.02 966.51 644.68 SP555 Ac-LTF$r8EY6clWAQL$AAAAAa-NH2 464 1963 983.28 1964.01 982.51 655.34 SP556 Ac-LTF$r8EF4bOH2WAQL$AAAAAa-NH2 465 1957.05 980.04 1958.06 979.53 653.36 SP557 Ac-AAALTF$r8EYWAQL$AAAAAa-NH2 466 2142.15 1072.83 2143.16 1072.08 715.06 SP558 Ac-LTF34F2$r8EYWAQL$AAAAAa-NH2 467 1965.02 984.3 1966.03 983.52 656.01 SP559 Ac-RTF$r8EYWAQL$AAAAAa-NH2 468 1972.06 987.81 1973.07 987.04 658.36 SP560 Ac-LTA$r8EYWAQL$AAAAAa-NH2 469 1853.01 928.33 1854.02 927.51 618.68 SP561 Ac-LTF$r8EYWAibQL$AAAAAa-NH2 470 1943.06 973.48 1944.07 972.54 648.69 SP562 Ac-LTF$r8EYWAQL$AAibAAAa-NH2 471 1943.06 973.11 1944.07 972.54 648.69 SP563 Ac-LTF$r8EYWAQL$AAAibAAa-NH2 472 1943.06 973.48 1944.07 972.54 648.69 SP564 Ac-LTF$r8EYWAQL$AAAAibAa-NH2 473 1943.06 973.48 1944.07 972.54 648.69 SP565 Ac-LTF$r8EYWAQL$AAAAAiba-NH2 474 1943.06 973.38 1944.07 972.54 648.69 SP566 Ac-LTF$r8EYWAQL$AAAAAiba-NH2 475 iso2 1943.06 973.38 1944.07 972.54 648.69 SP567 Ac-LTF$r8EYWAQL$AAAAAAib-NH2 476 1943.06 973.01 1944.07 972.54 648.69 SP568 Ac-LTF$r8EYWAQL$AaAAAa-NH2 477 1929.04 966.54 1930.05 965.53 644.02 SP569 Ac-LTF$r8EYWAQL$AAaAAa-NH2 478 1929.04 966.35 1930.05 965.53 644.02 SP570 Ac-LTF$r8EYWAQL$AAAaAa-NH2 479 1929.04 966.54 1930.05 965.53 644.02 SP571 Ac-LTF$r8EYWAQL$AAAaAa-NH2 480 iso2 1929.04 966.35 1930.05 965.53 644.02 SP572 Ac-LTF$r8EYWAQL$AAAAaa-NH2 481 1929.04 966.35 1930.05 965.53 644.02 SP573 Ac-LTF$r8EYWAQL$AAAAAA-NH2 482 1929.04 966.35 1930.05 965.53 644.02 SP574 Ac-LTF$r8EYWAQL$ASarAAAa-NH2 483 1929.04 966.54 1930.05 965.53 644.02 SP575 Ac-LTF$r8EYWAQL$AASarAAa-NH2 484 1929.04 966.35 1930.05 965.53 644.02 SP576 Ac-LTF$r8EYWAQL$AAASarAa-NH2 485 1929.04 966.35 1930.05 965.53 644.02 SP577 Ac-LTF$r8EYWAQL$AAAASara-NH2 486 1929.04 966.35 1930.05 965.53 644.02 SP578 Ac-LTF$r8EYWAQL$AAAAASar-NH2 487 1929.04 966.08 1930.05 965.53 644.02 SP579 Ac-7LTF$r8EYWAQL$AAAAAa-NH2 488 1918.07 951.99 1919.08 960.04 640.37 SP581 Ac-TF$r8EYWAQL$AAAAAa-NH2 489 1815.96 929.85 1816.97 908.99 606.33 SP582 Ac-F$r8EYWAQL$AAAAAa-NH2 490 1714.91 930.92 1715.92 858.46 572.64 SP583 Ac-LVF$r8EYWAQL$AAAAAa-NH2 491 1927.06 895.12 1928.07 964.54 643.36 SP584 Ac-AAF$r8EYWAQL$AAAAAa-NH2 492 1856.98 859.51 1857.99 929.5 620 SP585 Ac-LTF$r8EYWAQL$AAAAa-NH2 493 1858 824.08 1859.01 930.01 620.34 SP586 Ac-LTF$r8EYWAQL$AAAa-NH2 494 1786.97 788.56 1787.98 894.49 596.66 SP587 Ac-LTF$r8EYWAQL$AAa-NH2 495 1715.93 1138.57 1716.94 858.97 572.98 SP588 Ac-LTF$r8EYWAQL$Aa-NH2 496 1644.89 1144.98 1645.9 823.45 549.3 SP589 Ac-LTF$r8EYWAQL$a-NH2 497 1573.85 1113.71 1574.86 787.93 525.62 SP590 Ac-LTF$r8EYWAQL$AAA-OH 498 1716.91 859.55 1717.92 859.46 573.31 SP591 Ac-LTF$r8EYWAQL$A-OH 499 1574.84 975.14 1575.85 788.43 525.95 SP592 Ac-LTF$r8EYWAQL$AAA-NH2 500 1715.93 904.75 1716.94 858.97 572.98 SP593 Ac-LTF$r8EYWAQCba$SAA-OH 501 1744.91 802.49 1745.92 873.46 582.64 SP594 Ac-LTF$r8EYWAQCba$S-OH 502 1602.83 913.53 1603.84 802.42 535.28 SP595 Ac-LTF$r8EYWAQCba$S-NH2 503 1601.85 979.58 1602.86 801.93 534.96 SP596 4-FBzl-LTF$r8EYWAQL$AAAAAa-NH2 504 2009.05 970.52 2010.06 1005.53 670.69 SP597 4-FBzl-LTF$r8EYWAQCba$SAA-NH2 505 1823.93 965.8 1824.94 912.97 608.98 SP598 Ac-LTF$r8RYWAQL$AAAAAa-NH2 506 1956.1 988.28 1957.11 979.06 653.04 SP599 Ac-LTF$r8HYWAQL$AAAAAa-NH2 507 1937.06 1003.54 1938.07 969.54 646.69 SP600 Ac-LTF$r8QYWAQL$AAAAAa-NH2 508 1928.06 993.92 1929.07 965.04 643.69 SP601 Ac-LTF$r8CitYWAQL$AAAAAa-NH2 509 1957.08 987 1958.09 979.55 653.37 SP602 Ac-LTF$r8GlaYWAQL$AAAAAa-NH2 510 1973.03 983 1974.04 987.52 658.68 SP603 Ac-LTF$r8F4gYWAQL$AAAAAa-NH2 511 2004.1 937.86 2005.11 1003.06 669.04 SP604 Ac-LTF$r82mRYWAQL$AAAAAa-NH2 512 1984.13 958.58 1985.14 993.07 662.38 SP605 Ac-LTF$r8ipKYWAQL$AAAAAa-NH2 513 1970.14 944.52 1971.15 986.08 657.72 SP606 Ac-LTF$r8F4NH2YWAQL$AAAAAa-NH2 514 1962.08 946 1963.09 982.05 655.03 SP607 Ac-LTF$r8EYWAAL$AAAAAa-NH2 515 1872.02 959.32 1873.03 937.02 625.01 SP608 Ac-LTF$r8EYWALL$AAAAAa-NH2 516 1914.07 980.88 1915.08 958.04 639.03 SP609 Ac-LTF$r8EYWAAibL$AAAAAa-NH2 517 1886.03 970.61 1887.04 944.02 629.68 SP610 Ac-LTF$r8EYWASL$AAAAAa-NH2 518 1888.01 980.51 1889.02 945.01 630.34 SP611 Ac-LTF$r8EYWANL$AAAAAa-NH2 519 1915.02 1006.41 1916.03 958.52 639.35 SP612 Ac-LTF$r8EYWACitL$AAAAAa-NH2 520 1958.07 1959.08 980.04 653.7 SP613 Ac-LTF$r8EYWAHL$AAAAAa-NH2 521 1938.04 966.24 1939.05 970.03 647.02 SP614 Ac-LTF$r8EYWARL$AAAAAa-NH2 522 1957.08 1958.09 979.55 653.37 SP615 Ac-LTF$r8EpYWAQL$AAAAAa-NH2 523 2009.01 2010.02 1005.51 670.68 SP616 Cbm-LTF$r8EYWAQCba$SAA-NH2 524 1590.85 1591.86 796.43 531.29 SP617 Cbm-LTF$r8EYWAQL$AAAAAa-NH2 525 1930.04 1931.05 966.03 644.35 SP618 Ac-LTF$r8EYWAQL$SAAAAa-NH2 526 1945.04 1005.11 1946.05 973.53 649.35 SP619 Ac-LTF$r8EYWAQL$AAAASa-NH2 527 1945.04 986.52 1946.05 973.53 649.35 SP620 Ac-LTF$r8EYWAQL$SAAASa-NH2 528 1961.03 993.27 1962.04 981.52 654.68 SP621 Ac-LTF$r8EYWAQTba$AAAAAa-NH2 529 1943.06 983.1 1944.07 972.54 648.69 SP622 Ac-LTF$r8EYWAQAdm$AAAAAa-NH2 530 2007.09 990.31 2008.1 1004.55 670.04 SP623 Ac-LTF$r8EYWAQCha$AAAAAa-NH2 531 1969.07 987.17 1970.08 985.54 657.36 SP624 Ac-LTF$r8EYWAQhCha$AAAAAa-NH2 532 1983.09 1026.11 1984.1 992.55 662.04 SP625 Ac-LTF$r8EYWAQF$AAAAAa-NH2 533 1963.02 957.01 1964.03 982.52 655.35 SP626 Ac-LTF$r8EYWAQhF$AAAAAa-NH2 534 1977.04 1087.81 1978.05 989.53 660.02 SP627 Ac-LTF$r8EYWAQL$AANleAAa-NH2 535 1971.09 933.45 1972.1 986.55 658.04 SP628 Ac-LTF$r8EYWAQAdm$AANleAAa-NH2 536 2049.13 1017.97 2050.14 1025.57 684.05 SP629 4-FBz-BaLTF$r8EYWAQL$AAAAAa-NH2 537 2080.08 2081.09 1041.05 694.37 SP630 4-FBz-BaLTF$r8EYWAQCba$SAA-NH2 538 1894.97 1895.98 948.49 632.66 SP631 Ac-LTF$r5EYWAQL$s8AAAAAa-NH2 539 1929.04 1072.68 1930.05 965.53 644.02 SP632 Ac-LTF$r5EYWAQCba$s8SAA-NH2 540 1743.92 1107.79 1744.93 872.97 582.31 SP633 Ac-LTF$r8EYWAQL$AAhhLAAa-NH2 541 1999.12 2000.13 1000.57 667.38 SP634 Ac-LTF$r8EYWAQL$AAAAAAAa-NH2 542 2071.11 2072.12 1036.56 691.38 SP635 Ac-LTF$r8EYWAQL$AAAAAAAAa-NH2 543 2142.15 778.1 2143.16 1072.08 715.06 SP636 Ac-LTF$r8EYWAQL$AAAAAAAAAa-NH2 544 2213.19 870.53 2214.2 1107.6 738.74 SP637 Ac-LTA$r8EYAAQCba$SAA-NH2 545 1552.85 1553.86 777.43 518.62 SP638 Ac-LTA$r8EYAAQL$AAAAAa-NH2 546 1737.97 779.45 1738.98 869.99 580.33 SP639 Ac-LTF$r8EPmpWAQL$AAAAAa-NH2 547 2007.03 779.54 2008.04 1004.52 670.02 SP640 Ac-LTF$r8EPmpWAQCba$SAA-NH2 548 1821.91 838.04 1822.92 911.96 608.31 SP641 Ac-ATF$r8HYWAQL$S-NH2 549 1555.82 867.83 1556.83 778.92 519.61 SP642 Ac-LTF$r8HAWAQL$S-NH2 550 1505.84 877.91 1506.85 753.93 502.95 SP643 Ac-LTF$r8HYWAQA$S-NH2 551 1555.82 852.52 1556.83 778.92 519.61 SP644 Ac-LTF$r8EYWAQCba$SA-NH2 552 1672.89 887.18 1673.9 837.45 558.64 SP645 Ac-LTF$r8EYWAQL$SAA-NH2 553 1731.92 873.32 1732.93 866.97 578.31 SP646 Ac-LTF$r8HYWAQCba$SAA-NH2 554 1751.94 873.05 1752.95 876.98 584.99 SP647 Ac-LTF$r8SYWAQCba$SAA-NH2 555 1701.91 844.88 1702.92 851.96 568.31 SP648 Ac-LTF$r8RYWAQCba$SAA-NH2 556 1770.98 865.58 1771.99 886.5 591.33 SP649 Ac-LTF$r8KYWAQCba$SAA-NH2 557 1742.98 936.57 1743.99 872.5 582 SP650 Ac-LTF$r8QYWAQCba$SAA-NH2 558 1742.94 930.93 1743.95 872.48 581.99 SP651 Ac-LTF$r8EYWAACba$SAA-NH2 559 1686.9 1032.45 1687.91 844.46 563.31 SP652 Ac-LTF$r8EYWAQCba$AAA-NH2 560 1727.93 895.46 1728.94 864.97 576.98 SP653 Ac-LTF$r8EYWAQL$AAAAA-OH 561 1858.99 824.54 1860 930.5 620.67 SP654 Ac-LTF$r8EYWAQL$AAAA-OH 562 1787.95 894.48 1788.96 894.98 596.99 SP655 Ac-LTF$r8EYWAQL$AA-OH 563 1645.88 856 1646.89 823.95 549.63 SP656 Ac-LTF$r8AF4bOH2WAQL$AAAAAa-NH2 564 SP657 Ac-LTF$r8AF4bOH2WAAL$AAAAAa-NH2 565 SP658 Ac-LTF$r8EF4bOH2WAQCba$SAA-NH2 566 SP659 Ac-LTF$r8ApYWAQL$AAAAAa-NH2 567 SP660 Ac-LTF$r8ApYWAAL$AAAAAa-NH2 568 SP661 Ac-LTF$r8EpYWAQCba$SAA-NH2 569 SP662 Ac-LTF$rda6AYWAQL$da5AAAAAa-NH2 570 1974.06 934.44 SP663 Ac-LTF$rda6EYWAQCba$da5SAA-NH2 571 1846.95 870.52 869.94 SP664 Ac-LTF$rda6EYWAQL$da5AAAAAa-NH2 572 SP665 Ac-LTF$ra9EYWAQL$a6AAAAAa-NH2 573 936.57 935.51 SP666 Ac-LTF$ra9EYWAQL$a6AAAAAa-NH2 574 SP667 Ac-LTF$ra9EYWAQCba$a6SAA-NH2 575 SP668 Ac-LTA$ra9EYWAQCba$a6SAA-NH2 576 SP669 5-FAM-BaLTF$ra9EYWAQCba$a6SAA-NH2 577 SP670 5-FAM-BaLTF$r8EYWAQL$AAAAAa-NH2 578 2316.11 SP671 5-FAM-BaLTF$/r8EYWAQL$/AAAAAa-NH2 579 2344.15 SP672 5-FAM-BaLTA$r8EYWAQL$AAAAAa-NH2 580 2240.08 SP673 5-FAM-BaLTF$r8AYWAQL$AAAAAa-NH2 581 2258.11 SP674 5-FAM-BaATF$r8EYWAQL$AAAAAa-NH2 582 2274.07 SP675 5-FAM-BaLAF$r8EYWAQL$AAAAAa-NH2 583 2286.1 SP676 5-FAM-BaLTF$r8EAWAQL$AAAAAa-NH2 584 2224.09 SP677 5-FAM-BaLTF$r8EYAAQL$AAAAAa-NH2 585 2201.07 SP678 5-FAM-BaLTA$r8EYAAQL$AAAAAa-NH2 586 2125.04 SP679 5-FAM-BaLTF$r8EYWAAL$AAAAAa-NH2 587 2259.09 SP680 5-FAM-BaLTF$r8EYWAQA$AAAAAa-NH2 588 2274.07 SP681 5-FAM-BaLTF$/r8EYWAQCba$/ 589 2159.03 SAA-NH2 SP682 5-FAM-BaLTA$r8EYWAQCba$SAA-NH2 590 2054.97 SP683 5-FAM-BaLTF$r8EYAAQCba$SAA-NH2 591 2015.96 SP684 5-FAM-BaLTA$r8EYAAQCba$SAA-NH2 592 1939.92 SP685 5-FAM-BaQSQQTF$r8NLWRLL$QN-NH2 593 2495.23 SP686 5-TAMRA-BaLTF$r8EYWAQCba$SAA-NH2 594 2186.1 SP687 5-TAMRA-BaLTA$r8EYWAQCba$SAA-NH2 595 2110.07 SP688 5-TAMRA-BaLTF$r8EYAAQCba$SAA-NH2 596 2071.06 SP689 5-TAMRA-BaLTA$r8EYAAQCba$SAA-NH2 597 1995.03 SP690 5-TAMRA-BaLTF$/r8EYWAQCba$/ 598 2214.13 SAA-NH2 SP691 5-TAMRA-BaLTF$r8EYWAQL$AAAAAa-NH2 599 2371.22 SP692 5-TAMRA-BaLTA$r8EYWAQL$AAAAAa-NH2 600 2295.19 SP693 5-TAMRA-BaLTF$/r8EYWAQL$/ 601 2399.25 AAAAAa-NH2 SP694 Ac-LTF$r8EYWCou7QCba$SAA-OH 602 1947.93 SP695 Ac-LTF$r8EYWCou7QCba$S-OH 603 1805.86 SP696 Ac-LTA$r8EYWCou7QCba$SAA-NH2 604 1870.91 SP697 Ac-LTF$r8EYACou7QCba$SAA-NH2 605 1831.9 SP698 Ac-LTA$r8EYACou7QCba$SAA-NH2 606 1755.87 SP699 Ac-LTF$/r8EYWCou7QCba$/SAA-NH2 607 1974.98 SP700 Ac-LTF$r8EYWCou7QL$AAAAAa-NH2 608 2132.06 SP701 Ac-LTF$/r8EYWCou7QL$/AAAAAa-NH2 609 2160.09 SP702 Ac-LTF$r8EYWCou7QL$AAAAA-OH 610 2062A01 SP703 Ac-LTF$r8EYWCou7QL$AAAA-OH 611 1990.97 SP704 Ac-LTF$r8EYWCou7QL$AAA-OH 612 1919.94 SP705 Ac-LTF$r8EYWCou7QL$AA-OH 613 1848.9 SP706 Ac-LTF$r8EYWCou7QL$A-OH 614 1777.86 SP707 Ac-LTF$r8EYWAQL$AAAASa-NH2 615 iso2 974.4 973.53 SP708 Ac-LTF$r8AYWAAL$AAAAAa-NH2 616 iso2 1814.01 908.82 1815.02 908.01 605.68 SP709 Biotin-BaLTF$r8EYWAQL$AAAAAa-NH2 617 2184.14 1093.64 2185.15 1093.08 729.05 SP710 Ac-LTF$r8HAWAQL$S-NH2 618 iso2 1505.84 754.43 1506.85 753.93 502.95 SP711 Ac-LTF$r8EYWAQCba$SA-NH2 619 iso2 1672.89 838.05 1673.9 837.45 558.64 SP712 Ac-LTF$r8HYWAQCba$SAA-NH2 620 iso2 1751.94 877.55 1752.95 876.98 584.99 SP713 Ac-LTF$r8SYWAQCba$SAA-NH2 621 iso2 1701.91 852.48 1702.92 851.96 568.31 SP714 Ac-LTF$r8RYWAQCba$SAA-NH2 622 iso2 1770.98 887.45 1771.99 886.5 591.33 SP715 Ac-LTF$r8KYWAQCba$SAA-NH2 623 iso2 1742.98 872.92 1743.99 872.5 582 SP716 Ac-LTF$r8EYWAQCba$AAA-NH2 624 iso2 1727.93 865.71 1728.94 864.97 576.98 SP717 Ac-LTF$r8EYWAQL$AAAAAaBaC-NH2 625 2103.09 1053.12 2104.1 1052.55 702.04 SP718 Ac-LTF$r8EYWAQL$AAAAAadPeg4C-NH2 626 2279.19 1141.46 2280.2 1140.6 760.74 SP719 Ac-LTA$r8AYWAAL$AAAAAa-NH2 627 1737.98 870.43 1738.99 870 580.33 SP720 Ac-LTF$r8AYAAAL$AAAAAa-NH2 628 1698.97 851 1699.98 850.49 567.33 SP721 5-FAM-BaLTF$r8AYWAAL$AAAAAa-NH2 629 2201.09 1101.87 2202.1 1101.55 734.7 SP722 Ac-LTA$r8AYWAQL$AAAAAa-NH2 630 1795 898.92 1796.01 898.51 599.34 SP723 Ac-LTF$r8AYAAQL$AAAAAa-NH2 631 1755.99 879.49 1757 879 586.34 SP724 Ac-LTF$rda6AYWAAL$da5AAAAAa-NH2 632 1807.97 1808.98 904.99 603.66 SP725 FITC-BaLTF$r8EYWAQL$AAAAAa-NH2 633 2347.1 1174.49 2348.11 1174.56 783.37 SP726 FITC-BaLTF$r8EYWAQCba$SAA-NH2 634 2161.99 1082.35 2163 1082 721.67 SP733 Ac-LTF$r8EYWAQL$EAAAAa-NH2 635 1987.05 995.03 1988.06 994.53 663.36 SP734 Ac-LTF$r8AYWAQL$EAAAAa-NH2 636 1929.04 966.35 1930.05 965.53 644.02 SP735 Ac-LTF$r8EYWAQL$AAAAAaBaKbio-NH2 637 2354.25 1178.47 2355.26 1178.13 785.76 SP736 Ac-LTF$r8AYWAAL$AAAAAa-NH2 638 1814.01 908.45 1815.02 908.01 605.68 SP737 Ac-LTF$r8AYAAAL$AAAAAa-NH2 639 iso2 1698.97 850.91 1699.98 850.49 567.33 SP738 Ac-LTF$r8AYAAQL$AAAAAa-NH2 640 iso2 1755.99 879.4 1757 879 586.34 SP739 Ac-LTF$r8EYWAQL$EAAAAa-NH2 641 iso2 1987.05 995.21 1988.06 994.53 663.36 SP740 Ac-LTF$r8AYWAQL$EAAAAa-NH2 642 iso2 1929.04 966.08 1930.05 965.53 644.02 SP741 Ac-LTF$r8EYWAQCba$SAAAAa-NH2 643 1957.04 980.04 1958.05 979.53 653.35 SP742 Ac-LTF$r8EYWAQLStAAA$r5AA-NH2 644 2023.12 1012.83 2024.13 1012.57 675.38 SP743 Ac-LTF$r8EYWAQL$A$AAA$A-NH2 645 2108.17 1055.44 2109.18 1055.09 703.73 SP744 Ac-LTF$r8EYWAQL$AA$AAA$A-NH2 646 2179.21 1090.77 2180.22 1090.61 727.41 SP745 Ac-LTF$r8EYWAQL$AAA$AAA$A-NH2 647 2250.25 1126.69 2251.26 1126.13 751.09 SP746 Ac-AAALTF$r8EYWAQL$AAA-OH 648 1930.02 1931.03 966.02 644.35 SP747 Ac-AAALTF$r8EYWAQL$AAA-NH2 649 1929.04 965.85 1930.05 965.53 644.02 SP748 Ac-AAAALTF$r8EYWAQL$AAA-NH2 650 2000.08 1001.4 2001.09 1001.05 667.7 SP749 Ac-AAAAALTF$r8EYWAQL$AAA-NH2 651 2071.11 1037.13 2072.12 1036.56 691.38 SP750 Ac-AAAAAALTF$r8EYWAQL$AAA-NH2 652 2142.15 2143.16 1072.08 715.06 SP751 Ac-LTF$rda6EYWAQCba$da6SAA-NH2 653 iso2 1751.89 877.36 1752.9 876.95 584.97 SP752 Ac-t$r5wya$r5f4CF3ekllr-NH2 654 844.25 SP753 Ac-tawy$r5nf4CF3e$r5llr-NH2 655 837.03 SP754 Ac-tawya$r5f4CF3ek$r5lr-NH2 656 822.97 SP755 Ac-tawyanf4CF3e$r5llr$r5a-NH2 657 908.35 SP756 Ac-t$s8wyanf4CF3e$r5llr-NH2 658 858.03 SP757 Ac-tawy$s8nf4CF3ekll$r5a-NH2 659 879.86 SP758 Ac-tawya$s8f4CF3ekllr$r5a-NH2 660 936.38 SP759 Ac-tawy$s8naekll$r5a-NH2 661 844.25 SP760 5-FAM-Batawy$s8nf4CF3ekll$r5a-NH2 662 SP761 5-FAM-Batawy$s8naekll$r5a-NH2 663 SP762 Ac-tawy$s8nf4CF3eall$r5a-NH2 664 SP763 Ac-tawy$s8nf4CF3ekll$r5aaaaa-NH2 665 SP764 Ac-tawy$s8nf4CF3eall$r5aaaaa-NH2 666

Table 1a shows a selection of peptidomimetic macrocycles.

TABLE 1a  SEQ ID Exact Found Calc Calc Calc SP Sequence No: Isomer Mass Mass (M + 1)/1 (M + 2)/2 (M + 3)/3 SP244 Ac-LTF$r8EF4coohWAQCba$SANleA- 667 1885 943.59 1886.01 943.51 629.34 NH2 SP331 Ac-LTF$r8EYWAQL$AAAAAa-NH2 668 iso2 1929.04 966.08 1930.05 965.53 644.02 SP555 Ac-LTF$r8EY6clWAQL$AAAAAa-NH2 669 1963 983.28 1964.01 982.51 655.34 SP557 Ac-AAALTF$r8EYWAQL$AAAAAa-NH2 670 2142.15 1072.83 2143.16 1072.08 715.06 SP558 Ac-LTF34F2$r8EYWAQL$AAAAAa-NH2 671 1965.02 984.3 1966.03 983.52 656.01 SP562 Ac-LTF$r8EYWAQL$AAibAAAa-NH2 672 1943.06 973.11 1944.07 972.54 648.69 SP564 Ac-LTF$r8EYWAQL$AAAAibAa-NH2 673 1943.06 973.48 1944.07 972.54 648.69 SP566 Ac-LTF$r8EYWAQL$AAAAAiba-NH2 674 iso2 1943.06 973.38 1944.07 972.54 648.69 SP567 Ac-LTF$r8EYWAQL$AAAAAAib-NH2 675 1943.06 973.01 1944.07 972.54 648.69 SP572 Ac-LTF$r8EYWAQL$AAAAaa-NH2 676 1929.04 966.35 1930.05 965.53 644.02 SP573 Ac-LTF$r8EYWAQL$AAAAAA-NH2 677 1929.04 966.35 1930.05 965.53 644.02 SP578 Ac-LTF$r8EYWAQL$AAAAASar-NH2 678 1929.04 966.08 1930.05 965.53 644.02 SP551 Ac-LTF$r8EYWAQL$AAAAAa-OH 679 iso2 1930.02 965.89 1931.03 966.02 644.35 SP662 Ac-LTF$rda6AYWAQL$da5AAAAAa- 680 1974.06 934.44 933.49 NH2 SP367 5-FAM-BaLTF$r8EYWAQCba$SAA- 681 2131 1067.09 2132.01 1066.51 711.34 NH2 SP349 Ac-LTF$r8EF4coohWAQCba$AAAAAa- 682 iso2 1969.04 986.06 1970.05 985.53 657.35 NH2 SP347 Ac-LTF$r8EYWAQCba$AAAAAa-NH2 683 iso2 1941.04 972.55 1942.05 971.53 648.02

Table 1b shows a further selection of peptidomimetic macrocycles.

TABLE 1b  SEQ ID Iso- Exact Found Calc Calc Calc SP Sequence NO: mer Mass Mass (M + 1)/1 (M + 2)/2 (M + 3)/3 SP581 Ac-TF$r8EYWAQL$AAAAAa-NH2 684 1815.96 929.85 1816.97 908.99 606.33 SP582 Ac-F$r8EYWAQL$AAAAAa-NH2 685 1714.91 930.92 1715.92 858.46 572.64 SP583 Ac-LVF$r8EYWAQL$AAAAAa-NH2 686 1927.06 895.12 1928.07 964.54 643.36 SP584 Ac-AAF$r8EYWAQL$AAAAAa-NH2 687 1856.98 859.51 1857.99 929.5 620 SP585 Ac-LTF$r8EYWAQL$AAAAa-NH2 688 1858 824.08 1859.01 930.01 620.34 SP586 Ac-LTF$r8EYWAQL$AAAa-NH2 689 1786.97 788.56 1787.98 894.49 596.66 SP587 Ac-LTF$r8EYWAQL$AAa-NH2 690 1715.93 1138.57 1716.94 858.97 572.98 SP588 Ac-LTF$r8EYWAQL$Aa-NH2 691 1644.89 1144.98 1645.9 823.45 549.3 SP589 Ac-LTF$r8EYWAQL$a-NH2 692 1573.85 1113.71 1574.86 787.93 525.62

In the sequences shown above and elsewhere, the following abbreviations are used: “Nle” represents norleucine, “Aib” represents 2-aminoisobutyric acid, “Ac” represents acetyl, and “Pr” represents propionyl Amino acids represented as “$” are alpha-Me S5-pentenyl-alanine olefin amino acids connected by an all-carbon crosslinker comprising one double bond Amino acids represented as “$r5” are alpha-Me R5-pentenyl-alanine olefin amino acids connected by an all-carbon comprising one double bond Amino acids represented as “$s8” are alpha-Me S8-octenyl-alanine olefin amino acids connected by an all-carbon crosslinker comprising one double bond. Amino acids represented as “$r8” are alpha-Me R8-octenyl-alanine olefin amino acids connected by an all-carbon crosslinker comprising one double bond. “Ahx” represents an aminocyclohcxyl linker. The crosslinkers are linear all-carbon crosslinker comprising eight or eleven carbon atoms between the alpha carbons of each amino acid Amino acids represented as “$/” are alpha-Me S5-pentenyl-alanine olefin amino acids that are not connected by any crosslinker Amino acids represented as “$/r5” are alpha-Me R5-pentenyl-alanine olefin amino acids that are not connected by any crosslinker Amino acids represented as “$/s8” are alpha-Me S8-octenyl-alanine olefin amino acids that are not connected by any crosslinker Amino acids represented as “$/r8” are alpha-Me R8-octenyl-alanine olefin amino acids that are not connected by any crosslinker. Amino acids represented as “Amw” are alpha-Me tryptophan amino acids Amino acids represented as “Aml” are alpha-Me leucine amino acids. Amino acids represented as “Amf” are alpha-Me phenylalanine amino acids Amino acids represented as “2ff” are 2-fluoro-phenylalanine amino acids. Amino acids represented as “3ff” are 3-fluoro-phenylalanine amino acids. Amino acids represented as “St” are amino acids comprising two pentenyl-alanine olefin side chains, each of which is crosslinked to another amino acid as indicated Amino acids represented as “St//” are amino acids comprising two pentenyl-alanine olefin side chains that are not crosslinked. Amino acids represented as “% St” are amino acids comprising two pentenyl-alaninc olefin side chains, each of which is crosslinked to another amino acid as indicated via fully saturated hydrocarbon crosslinks. Amino acids represented as “Ba” are beta-alanine. The lower-case character “e” or “z” within the designation of a crosslinked amino acid (e.g. “$er8” or “Szr8”) represents the configuration of the double bond (E or Z, respectively). In other contexts, lower-case letters such as “a” or “f” represent D amino acids (e.g. D-alanine, or D-phenylalanine, respectively). Amino acids designated as “NmW” represent N-methyltryptophan Amino acids designated as “NmY” represent N-methyltyrosine Amino acids designated as “NmA” represent N-methylalanine. “Kbio” represents a biotin group attached to the side chain amino group of a lysine residue. Amino acids designated as “Sar” represent sarcosine Amino acids designated as “Cha” represent cyclohexyl alanine Amino acids designated as “Cpg” represent cyclopentyl glycine. Amino acids designated as “Chg” represent cyclohexyl glycine Amino acids designated as “Cba” represent cyclobutyl alanine Amino acids designated as “F41” represent 4-iodo phenylalanine. “7L” represents N15 isotopic leucine Amino acids designated as “F3Cl” represent 3-chloro phenylalanine. Amino acids designated as “F4cooh” represent 4-carboxy phenylalanine Amino acids designated as “F34F2” represent 3,4-difluoro phenylalanine Amino acids designated as “6clW” represent 6-chloro tryptophan. Amino acids designated as “$rda6” represent alpha-Me R6-hexynyl-alanine alkynyl amino acids, crosslinked via a dialkyne bond to a second alkynyl amino acid Amino acids designated as “$da5” represent alpha-Me S5-pentynyl-alanine alkynyl amino acids, wherein the alkyne forms one half of a dialkyne bond with a second alkynyl amino acid Amino acids designated as “$ra9” represent alpha-Mc R9-nonynyl-alaninc alkynyl amino acids, crosslinked via an alkyne metathesis reaction with a second alkynyl amino acid Amino acids designated as “$a6” represent alpha-Me S6-hexynyl-alanine alkynyl amino acids, crosslinked via an alkyne metathesis reaction with a second alkynyl amino acid. The designation “iso1” or “iso2” indicates that the peptidomimetic macrocycle is a single isomer.

Amino acids designated as “Cit” represent citrulline Amino acids designated as “Cou4”, “Cou6”, “Cou7” and “Cou8”, respectively, represent the following structures:

In some embodiments, a peptidomimetic macrocycle is obtained in more than one isomer, for example due to the configuration of a double bond within the structure of the crosslinker (E vs Z). Such isomers can or can not be separable by conventional chromatographic methods. In some embodiments, one isomer has improved biological properties relative to the other isomer. In one embodiment, an E crosslinker olefin isomer of a peptidomimetic macrocycle has better solubility, better target affinity, better in vivo or in vitro efficacy, higher helicity, or improved cell permeability relative to its Z counterpart. In another embodiment, a Z crosslinker olefin isomer of a peptidomimetic macrocycle has better solubility, better target affinity, better in vivo or in vitro efficacy, higher hclicity, or improved cell permeability relative to its E counterpart.

Table 1c shows exemplary peptidomimetic macrocycle:

TABLE 1c Structure SP154 (SEQ ID NO: 163)

  Chemical Formula: C₈₇H₁₂₅N₁₇O₂₁ Exact Mass: 1743.92 Molecular Weight: 1745.02 Ac-L T F $er8 E YWAQCba $e SAA-NH2 SP115 (SEQ ID NO: 124)

  Chemical Formula: C₈₅H₁₂₅N₁₇O₁₉ Exact Mass: 1687.93 Molecular Weight: 1689.00 Ac-L T F $er8 AYWAQhL $e SAA-NH2 SP114 (SEQ ID NO: 123)

  Chemical Formula: C₈₅H₁₂₅N₁₇O₁₉ Exact Mass: 1687.93 Molecular Weight: 1689.00 Ac-L T F $zr8 AYWAQhL $z SAA-NH2 SP99 (SEQ ID NO: 108)

  Chemical Formula: C₈₄H₁₂₂ClN₁₇O₁₉ Exact Mass: 1707.88 Molecular Weight: 1709.42 Ac-L T F $er8 AY6clWAQL $e SAA-NH2 SP388 (SEQ ID NO: 397)

  Chemical Formula: C₉₁H₁₃₆N₁₈O₁₉ Exact Mass: 1785.02 Molecular Weight: 1786.16 Ac-L T F $er8 AYAmwAQL $e AA Nle A-NH2 SP331 (SEQ ID NO: 340)

  Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 Ac-L T F $er8 EYWAQL $e AA A A A a-NH2 SP445 (SEQ ID NO: 454)

  Chemical Formula: C₉₅H₁₄₂N₂₀O₂₃ Exact Mass: 1931.06 Molecular Weight: 1932.26 Ac-L T F %r8 EYWAQL % AA A A A a-NH2 SP351 (SEQ ID NO: 360)

  Chemical Formula: C₉₆H₁₄₀N₂₀O₂₄ Exact Mass: 1957.03 Molecular Weight: 1958.26 Ac-L T F $er8 E YWSQCba $eA A A A A a-NH2 SP71 (SEQ ID NO: 80)

  Chemical Formula: C₉₀H₁₃₄N₁₈O₁₉ Exact Mass: 1771.01 Molecular Weight: 1772.14 Ac-L T F $er8 A YWAQL$e AA I a-NH2 SP69 (SEQ ID NO: 78)

  Chemical Formula: C₉₀H₁₃₄N₁₈O₁₉ Exact Mass: 1771.01 Molecular Weight: 1772.14 Ac-L T F $er8 AYWAQL $eAA Nle A-NH2 SP7 (SEQ ID NO: 16)

  Chemical Formula: C₉₀H₁₂₇N₁₇O₁₉ Exact Mass: 1749.95 Molecular Weight: 1751.07 Ac-L T F $r8 AYWAQL $ SA F-NH2 SP160 (SEQ ID NO: 169)

  Chemical Formula: C₈₇H₁₂₅F₂N₁₇O₂₁ Exact Mass: 1781.92 Molecular Weight: 1783.02 Ac-L T F34F2 $er8 EYWAQhL $e SAA-NH2 SP315 (SEQ ID NO: 324)

  Chemical Formula: C₉₃H₁₃₈N₂₀O₂₁ Exact Mass: 1871.03 Molecular Weight: 1872.21 Ac-L T F $er8 AYWAQL$eAA A A A a-NH2 SP249 (SEQ ID NO: 258)

  Chemical Formula: C₉₄H₁₃₆N₁₈O₂₂ Exact Mass: 1869.01 Molecular Weight: 1870.19 Ac-L T F $er8 E F4coohWAQCba $e AA-I-a-NH2 SP437 (SEQ ID NO: 446)

  Chemical Formula: C₉₅H₁₄₃N₂₁O₂₁ Exact Mass: 1914.08 Molecular Weight: 1915.28 Dmaac-L T F $er8 AYWAQL$eAA A A A a-NH2 SP349 (SEQ ID NO: 358)

  Chemical Formula: C₉₇H₁₄₀N₂₀O₂₄ Exact Mass: 1969.03 Molecular Weight: 1970.27 Ac-L T F $er8 E F4coohWAQCba$e A A A A A a-NH2 SP555 (SEQ ID NO: 464)

  Chemical Formula: C₉₅H₁₃₉ClN₂₀O₂₃ Exact Mass: 1963.00 Molecular Weight: 1964.69 Ac-L T F$er8 EY6clWAQL$eAA A A A a-NH2 SP557 (SEQ ID NO: 466)

  Chemical Formula: C₁₀₄H₁₅₅N₂₃O₂₆ Exact Mass: 2142.15 Molecular Weight: 2143.48 Ac-A A A L T F $er8 E YWAQL$e AA A A A a-NH2 SP558 (SEQ ID NO: 467)

  Chemical Formula: C₉₅H₁₃₈F₂N₂₀O₂₃ Exact Mass: 1965.02 Molecular Weight: 1966.23 Ac-L T F34F2 $er8 E YWAQL $e AAA AA a-NH2 SP367 (SEQ ID NO: 376)

  5-FAM-Ba L T F $er8 EYWAQCba $e SAA-NH2 SP562 (SEQ ID NO: 471)

  Chemical Formula: C₉₆H₁₄₂N₂₀O₂₃ Exact Mass: 1943.06 Molecular Weight: 1944.27 Ac-LT F $er8 E YWAQL$eAAib A A A a-NH2 SP564 (SEQ ID NO: 473)

  Chemical Formula: C₉₆H₁₄₂N₂₀O₂₃ Exact Mass: 1943.06 Molecular Weight: 1944.27 Ac-L T F $er8 E YWAQL $e AA A Aib A a-NH2 SP566 (SEQ ID NO: 475)

SP567 (SEQ ID NO: 476)

  Chemical Formula: C₉₆H₁₄₂N₂₀O₂₃ Exact Mass: 1943.06 Molecular Weight: 1944.27 Ac-L T F $er8 EYWAQL $e AA A A A Aib-NH2 SP572 (SEQ ID NO: 481)

  Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 Ac-L T F $er8 E YWAQL $e AA A A a a-NH2 SP573 (SEQ ID NO: 482)

  Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 Ac-L T F $er8 E YWAQL $eAA A A A A-NH2 SP578 (SEQ ID NO: 487)

  Chemical Formula: C₉₅H₁₄₀N₂₀O₂₃ Exact Mass: 1929.04 Molecular Weight: 1930.25 Ac-LT F $er8 E YWAQL$eAA A A A Sar-NH2 SP664 (SEQ ID NO: 572)

  Chemical Formula: C₉₅H₁₃₄N₂₀O₂₃ Exact Mass: 1922.99 Molecular Weight: 1924.20 Ac-LTF$rda6EYWAQL$da5AAAAAa-NH2 SP664 (SEQ ID NO: 572)

  Chemical Formula: C₉₅H₁₃₄N₂₀O₂₃ Exact Mass: 1922.99 Molecular Weight: 1924.20 Ac-L T F $rda6 E YWAQL$da5 AA A AA a-NH2 (SEQ ID NO: 1500)

  Chemical Formula: C₉₆H₁₃₆N₂₀O₂₃ Exact Mass: 1937.01 Molecular Weight: 1938.23

In some embodiments, peptidomimetic macrocycles exclude peptidomimetic macrocycles shown in Table 2a:

TABLE 2a  Number Sequence SEQ ID NO: 1 L$r5QETFSD$s8WKLLPEN 693 2 LSQ$r5TFSDLW$s8LLPEN 694 3 LSQE$r5FSDLWK$s8LPEN 695 4 LSQET$r5SDLWKL$s8PEN 696 5 LSQETF$r5DLWKLL$s8EN 697 6 LXQETFS$r5LWKLLP$s8N 698 7 LSQETFSD$r5WKLLPE$s8 699 8 LSQQTF$r5DLWKLL$s8EN 700 9 LSQETF$r5DLWKLL$s8QN 701 10 LSQQTF$r5DLWKLL$s8QN 702 11 LSQETF$r5NLWKLL$s8QN 703 12 LSQQTF$r5NLWKLL$s8QN 704 13 LSQQTF$r5NLWRLL$s8QN 705 14 QSQQTF$r5NLWKLL$s8QN 706 15 QSQQTF$r5NLWRLL$s8QN 707 16 QSQQTA$r5NLWRLL$s8QN 708 17 L$r8QETFSD$WKLLPEN 709 18 LSQ$r8TFSDLW$LLPEN 710 19 LSQE$r8FSDLWK$LPEN 711 20 LSQET$r8SDLWKL$PEN 712 21 LSQETF$r8DLWKLL$EN 713 22 LXQETFS$r8LWKLLP$N 714 23 LSQETFSD$r8WKLLPE$ 715 24 LSQQTF$r8DLWKLL$EN 716 25 LSQETF$r8DLWKLL$QN 717 26 LSQQTF$r8DLWKLL$QN 718 27 LSQETF$r8NLWKLL$QN 719 28 LSQQTF$r8NLWKLL$QN 720 29 LSQQTF$r8NLWRLL$QN 721 30 QSQQTF$r8NLWKLL$QN 722 31 QSQQTF$r8NLWRLL$QN 723 32 QSQQTA$r8NLWRLL$QN 724 33 QSQQTF$r8NLWRKK$QN 725 34 QQTF$r8DLWRLL$EN 726 35 QQTF$r8DLWRLL$ 727 36 LSQQTF$DLW$LL 728 37 QQTF$DLW$LL 729 38 QQTA$r8DLWRLL$EN 730 39 QSQQTF$r5NLWRLL$s8QN 731 (dihydroxylated olefin) 40 QSQQTA$r5NLWRLL$s8QN 732 (dihydroxylated olefin) 41 QSQQTF$r8DLWRLL$QN 733 42 QTF$r8NLWRLL$ 734 43 QSQQTF$NLW$LLPQN 735 44 QS$QTF$NLWRLLPQN 736 45 $TFS$LWKLL 737 46 ETF$DLW$LL 738 47 QTF$NLW$LL 739 48 $SQE$FSNLWKLL 740

In Table 2a, X represents S or any amino acid. Peptides shown can comprise an N-terminal capping group such as acetyl or an additional linker such as beta-alanine between the capping group and the start of the peptide sequence.

In some embodiments, peptidomimetic macrocycles do not comprise a peptidomimetic macrocycle structure as shown in Table 2a.

In other embodiments, peptidomimetic macrocycles exclude peptidomimetic macrocycles shown in Table 2b:

TABLE 2b SEQ ID Exact Observed Number Sequence NO: Mass M + 2 mass (m/e) 1 Ac-LSQETF$r8DLWKLL$EN-NH2 741 2068.13 1035.07 1035.36 2 Ac-LSQETF$r8NLWKLL$QN-NH2 742 2066.16 1034.08 1034.31 3 Ac-LSQQTF$r8NLWRLL$QN-NH2 743 2093.18 1047.59 1047.73 4 Ac-QSQQTF$r8NLWKLL$QN-NH2 744 2080.15 1041.08 1041.31 5 Ac-QSQQTF$r8NLWRLL$QN-NH2 745 2108.15 1055.08 1055.32 6 Ac-QSQQTA$r8NLWRLL$QN-NH2 746 2032.12 1017.06 1017.24 7 Ac-QAibQQTF$r8NLWRLL$QN-NH2 747 2106.17 1054.09 1054.34 8 Ac-QSQQTFSNLWRLLPQN-NH2 748 2000.02 1001.01 1001.26 9 Ac-QSQQTF$/r8NLWRLL$/QN-NH2 749 2136.18 1069.09 1069.37 10 Ac-QSQAibTF$r8NLWRLL$QN-NH2 750 2065.15 1033.58 1033.71 11 Ac-QSQQTF$r8NLWRLL$AN-NH2 751 2051.13 1026.57 1026.70 12 Ac-ASQQTF$r8NLWRLL$QN-NH2 752 2051.13 1026.57 1026.90 13 Ac-QSQQTF$r8ALWRLL$QN-NH2 753 2065.15 1033.58 1033.41 14 Ac-QSQETF$r8NLWRLL$QN-NH2 754 2109.14 1055.57 1055.70 15 Ac-RSQQTF$r8NLWRLL$QN-NH2 755 2136.20 1069.10 1069.17 16 Ac-RSQQTF$r8NLWRLL$EN-NH2 756 2137.18 1069.59 1069.75 17 Ac-LSQETFSDLWKLLPEN-NH2 757 1959.99 981.00 981.24 18 Ac-QSQ$TFS$LWRLLPQN-NH2 758 2008.09 1005.05 1004.97 19 Ac-QSQQ$FSN$WRLLPQN-NH2 759 2036.06 1019.03 1018.86 20 Ac-QSQQT$SNL$RLLPQN-NH2 760 1917.04 959.52 959.32 21 Ac-QSQQTF$NLW$LLPQN-NH2 761 2007.06 1004.53 1004.97 22 Ac-RTQATF$r8NQWAibANle$TNAibTR- 762 2310.26 1156.13 1156.52 NH2 23 Ac-QSQQTF$r8NLWRLL$RN-NH2 763 2136.20 1069.10 1068.94 24 Ac-QSQRTF$r8NLWRLL$QN-NH2 764 2136.20 1069.10 1068.94 25 Ac-QSQQTF$r8NNleWRLL$QN-NH2 765 2108.15 1055.08 1055.44 26 Ac-QSQQTF$r8NLWRNleL$QN-NH2 766 2108.15 1055.08 1055.84 27 Ac-QSQQTF$r8NLWRLNle$QN-NH2 767 2108.15 1055.08 1055.12 28 Ac-QSQQTY$r8NLWRLL$QN-NH2 768 2124.15 1063.08 1062.92 29 Ac-RAibQQTF$r8NLWRLL$QN-NH2 769 2134.22 1068.11 1068.65 30 Ac-MPRFMDYWEGLN-NH2 770 1598.70 800.35 800.45 31 Ac-RSQQRF$r8NLWRLL$QN-NH2 771 2191.25 1096.63 1096.83 32 Ac-QSQQRF$r8NLWRLL$QN-NH2 772 2163.21 1082.61 1082.87 33 Ac-RAibQQRF$r8NLWRLL$QN-NH2 773 2189.27 1095.64 1096.37 34 Ac-RSQQRF$r8NFWRLL$QN-NH2 774 2225.23 1113.62 1114.37 35 Ac-RSQQRF$r8NYWRLL$QN-NH2 775 2241.23 1121.62 1122.37 36 Ac-RSQQTF$r8NLWQLL$QN-NH2 776 2108.15 1055.08 1055.29 37 Ac-QSQQTF$r8NLWQAmlL$QN-NH2 777 2094.13 1048.07 1048.32 38 Ac-QSQQTF$r8NAmlWRLL$QN-NH2 778 2122.17 1062.09 1062.35 39 Ac-NlePRF$r8DYWEGL$QN-NH2 779 1869.98 935.99 936.20 40 Ac-NlePRF$r8NYWRLL$QN-NH2 780 1952.12 977.06 977.35 41 Ac-RF$r8NLWRLL$Q-NH2 781 1577.96 789.98 790.18 42 Ac-QSQQTF$r8N2ffWRLL$QN-NH2 782 2160.13 1081.07 1081.40 43 Ac-QSQQTF$r8N3ffWRLL$QN-NH2 783 2160.13 1081.07 1081.34 44 Ac-QSQQTF#r8NLWRLL#QN-NH2 784 2080.12 1041.06 1041.34 45 Ac-RSQQTA$r8NLWRLL$QN-NH2 785 2060.16 1031.08 1031.38 46 Ac-QSQQTF%r8NLWRLL%QN-NH2 786 2110.17 1056.09 1056.55 47 HepQSQ$TFSNLWRLLPQN-NH2 787 2051.10 1026.55 1026.82 48 HepQSQ$TF$r8NLWRLL$QN-NH2 788 2159.23 1080.62 1080.89 49 Ac-QSQQjF$r8NL6clWRLL$QN-NH2 789 2142.11 1072.06 1072.35 50 Ac-QSQQjF$r8NLMe6clwRLL$QN-NH2 790 2156.13 1079.07 1079.27 51 Ac-LTFEHYWAQLTS-NH2 791 1535.74 768.87 768.91 52 Ac-LTF$HYW$QLTS-NH2 792 1585.83 793.92 794.17 53 Ac-LTFE$YWA$LTS-NH2 793 1520.79 761.40 761.67 54 Ac-LTF$zr8HYWAQL$zS-NH2 794 1597.87 799.94 800.06 55 Ac-LTF$r8HYWRQL$S-NH2 795 1682.93 842.47 842.72 56 Ac-QS$QTFStNLWRLL$s8QN-NH2 796 2145.21 1073.61 1073.90 57 Ac-QSQQTASNLWRLLPQN-NH2 797 1923.99 963.00 963.26 58 Ac-QSQQTA$/r8NLWRLL$/QN-NH2 798 2060.15 1031.08 1031.24 59 Ac-ASQQTF$/r8NLWRLL$/QN-NH2 799 2079.16 1040.58 1040.89 60 Ac-$SQQ$FSNLWRLLAibQN-NH2 800 2009.09 1005.55 1005.86 61 Ac-QS$QTF$NLWRLLAibQN-NH2 801 2023.10 1012.55 1012.79 62 Ac-QSQQ$FSN$WRLLAibQN-NH2 802 2024.06 1013.03 1013.31 63 Ac-QSQQTF$NLW$LLAibQN-NH2 803 1995.06 998.53 998.87 64 Ac-QSQQTFS$LWR$LAibQN-NH2 804 2011.06 1006.53 1006.83 65 Ac-QSQQTFSNLW$LLA$N-NH2 804 1940.02 971.01 971.29 66 Ac-$/SQQ$/FSNLWRLLAibQN-NH2 806 2037.12 1019.56 1019.78 67 Ac-QS$/QTF$/NLWRLLAibQN-NH2 807 2051.13 1026.57 1026.90 68 Ac-QSQQ$/FSN$/WRLLAibQN-NH2 808 2052.09 1027.05 1027.36 69 Ac-QSQQTF$/NLW$/LLAibQN-NH2 809 2023.09 1012.55 1013.82 70 Ac-QSQ$TFS$LWRLLAibQN-NH2 810 1996.09 999.05 999.39 71 Ac-QSQ$/TFS$/LWRLLAibQN-NH2 811 2024.12 1013.06 1013.37 72 Ac-QS$/QTFSt//NLWRLL$/s8QN-NH2 812 2201.27 1101.64 1102.00 73 Ac-$r8SQQTFS$LWRLLAibQN-NH2 813 2038.14 1020.07 1020.23 74 Ac-QSQ$r8TFSNLW$LLAibQN-NH2 814 1996.08 999.04 999.32 75 Ac-QSQQTFS$r8LWRLLA$N-NH2 815 2024.12 1013.06 1013.37 76 Ac-QS$r5QTFStNLW$LLAibQN-NH2 816 2032.12 1017.06 1017.39 77 Ac-$/r8SQQJFS$/LWRLLAibQN-NH2 817 2066.17 1034.09 1034.80 78 Ac-QSQ$/r8TFSNLW$/LLAibQN-NH2 818 2024.11 1013.06 1014.34 79 Ac-QSQQTFS$/r8LWRLLA$/N-NH2 819 2052.15 1027.08 1027.16 80 Ac-QS$/r5QTFSt//NLW$/LLAibQN-NH2 820 2088.18 1045.09 1047.10 81 Ac-QSQQTFSNLWRLLAibQN-NH2 821 1988.02 995.01 995.31 82 Hep/QSQ$/TF$/r8NLWRLL$/QN-NH2 822 2215.29 1108.65 1108.93 83 Ac-ASQQTF$r8NLRWLL$QN-NH2 823 2051.13 1026.57 1026.90 84 Ac-QSQQjF$/r8NLWRLL$/Q-NH2 824 2022.14 1012.07 1012.66 85 Ac-QSQQTF$r8NLWRLL$Q-NH2 825 1994.11 998.06 998.42 86 Ac-AAARAA$r8AAARAA$AA-NH2 826 1515.90 758.95 759.21 87 Ac-LTFEHYWAQLTSA-NH2 827 1606.78 804.39 804.59 88 Ac-LTF$r8HYWAQL$SA-NH2 828 1668.90 835.45 835.67 89 Ac-ASQQTFSNLWRLLPQN-NH2 829 1943.00 972.50 973.27 90 Ac-QS$QTFStNLW$r5LLAibQN-NH2 830 2032.12 1017.06 1017.30 91 Ac-QSQQTFAibNLWRLLAibQN-NH2 831 1986.04 994.02 994.19 92 Ac-QSQQTFNleNLWRLLNleQN-NH2 832 2042.11 1022.06 1022.23 93 Ac-QSQQTF$/r8NLWRLLAibQN-NH2 833 2082.14 1042.07 1042.23 94 Ac-QSQQTF$/r8NLWRLLNleQN-NH2 834 2110.17 1056.09 1056.29 95 Ac-QSQQTFAibNLWRLL$/QN-NH2 835 2040.09 1021.05 1021.25 96 Ac-QSQQTFNleNLWRLL$/QN-NH2 836 2068.12 1035.06 1035.31 97 Ac-QSQQTF%r8NL6clWRNleL%QN-NH2 837 2144.13 1073.07 1073.32 98 Ac-QSQQTF%r8NLMe6clWRLL%QN-NH2 838 2158.15 1080.08 1080.31 101 Ac-FNle$YWE$L-NH2 839 1160.63 — 1161.70 102 Ac-F$r8AYWELL$A-NH2 840 1344.75 — 1345.90 103 Ac-F$r8AYWQLL$A-NH2 841 1343.76 — 1344.83 104 Ac-NlePRF$r8NYWELL$QN-NH2 842 1925.06 963.53 963.69 105 Ac-NlePRF$r8DYWRLL$QN-NH2 843 1953.10 977.55 977.68 106 Ac-NlePRF$r8NYWRLL$Q-NH2 844 1838.07 920.04 920.18 107 Ac-NlePRF$r8NYWRLL$-NH2 845 1710.01 856.01 856.13 108 Ac-QSQQTF$r8DLWRLL$QN-NH2 846 2109.14 1055.57 1055.64 109 Ac-QSQQTF$r8NLWRLL$EN-NH2 847 2109.14 1055.57 1055.70 110 Ac-QSQQTF$r8NLWRLL$QD-NH2 848 2109.14 1055.57 1055.64 111 Ac-QSQQTF$r8NLWRLL$S-NH2 849 1953.08 977.54 977.60 112 Ac-ESQQTF$r8NLWRLL$QN-NH2 850 2109.14 1055.57 1055.70 113 Ac-LTF$r8NLWRNleL$Q-NH2 851 1635.99 819.00 819.10 114 Ac-LRF$r8NLWRNleL$Q-NH2 852 1691.04 846.52 846.68 115 Ac-QSQQTF$r8NWWRNleL$QN-NH2 853 2181.15 1091.58 1091.64 116 Ac-QSQQTF$r8NLWRNleL$Q-NH2 854 1994.11 998.06 998.07 117 Ac-QTF$r8NLWRNleL$QN-NH2 855 1765.00 883.50 883.59 118 Ac-NlePRF$r8NWWRLL$QN-NH2 856 1975.13 988.57 988.75 119 Ac-NlePRF$r8NWWRLL$A-NH2 857 1804.07 903.04 903.08 120 Ac-TSFAEYWNLLNH2 858 1467.70 734.85 734.90 121 Ac-QTF$r8HWWSQL$S-NH2 859 1651.85 826.93 827.12 122 Ac-FM$YWE$L-NH2 860 1178.58 — 1179.64 123 Ac-QTFEHWWSQLLS-NH2 861 1601.76 801.88 801.94 124 Ac-QSQQTF$r8NLAmwRLNle$QN-NH2 862 2122.17 1062.09 1062.24 125 Ac-FMAibY6clWEAc3cL-NH2 863 1130.47 — 1131.53 126 Ac-FNle$Y6clWE$L-NH2 864 1194.59 — 1195.64 127 Ac-F$zr8AY6clWEAc3cL$z-NH2 865 1277.63 639.82 1278.71 128 Ac-F5r8AY6clWEAc3cL$A-NH2 866 1348.66 — 1350.72 129 Ac-NlePRF$r8NY6clWRLL$QN-NH2 867 1986.08 994.04 994.64 130 Ac-AF$r8AAWALA$A-NH2 868 1223.71 — 1224.71 131 Ac-TF$r8AAWRLA$Q-NH2 869 1395.80 698.90 399.04 132 Pr-TF$r8AAWRLA$Q-NH2 870 1409.82 705.91 706.04 133 Ac-QSQQTF%r8NLWRNleL%QN-NH2 871 2110.17 1056.09 1056.22 134 Ac-LTF%r8HYWAQL%SA-NH2 872 1670.92 836.46 836.58 135 Ac-NlePRF%r8NYWRLL%QN-NH2 873 1954.13 978.07 978.19 136 Ac-NlePRF%r8NY6clWRLL%QN-NH2 874 1988.09 995.05 995.68 137 Ac-LTF%r8HY6clWAQL%S-NH2 875 1633.84 817.92 817.93 138 Ac-QS%QTF%StNLWRLL%s8QN-NH2 876 2149.24 1075.62 1075.65 139 Ac-LTF%r8HY6clWRQL%S-NH2 877 1718.91 860.46 860.54 140 Ac-QSQQTF%r8NL6clWRLL%QN-NH2 878 2144.13 1073.07 1073.64 141 Ac-%r8SQQTFS%LWRLLAibQN-NH2 879 2040.15 1021.08 1021.13 142 Ac-LTF%r8HYWAQL%S-NH2 880 1599.88 800.94 801.09 143 Ac-TSF%r8QYWNLL%P-NH2 881 1602.88 802.44 802.58 147 Ac-LTFEHYWAQLTS-NH2 882 1535.74 768.87 769.5 152 Ac-F$er8AY6clWEAc3cL$e-NH2 883 1277.63 639.82 1278.71 153 Ac-AF5r8AAWALASA-NH2 884 1277.63 639.82 1277.84 154 Ac-TF$r8AAWRLA$Q-NH2 885 1395.80 698.90 699.04 155 Pr-TF$r8AAWRLA$Q-NH2 886 1409.82 705.91 706.04 156 Ac-LTFSer8HYWAQLSeS-NH2 887 1597.87 799.94 800.44 159 Ac-CCPGCCBaQSQQTF$r8NLWRLL$QN-NH2 888 2745.30 1373.65 1372.99 160 Ac-CCPGCCBaQSQQTA$r8NLWRLL$QN-NH2 889 2669.27 1335.64 1336.09 161 Ac-CCPGCCBaNlePRF$r8NYWRLL$QN-NH2 890 2589.26 1295.63 1296.2 162 Ac-LTF$/r8HYWAQLS/S-NH2 891 1625.90 813.95 814.18 163 Ac-F%r8HY6clWRAc3cL%-NH2 892 1372.72 687.36 687.59 164 Ac-QTF%r8HWWSQL%S-NH2 893 1653.87 827.94 827.94 165 Ac-LTA$r8HYWRQL$S-NH2 894 1606.90 804.45 804.66 166 Ac-C4r8QQTFSN$WRLLAibQN-NH2 895 2080.12 1041.06 1041.61 167 Ac-QSQQ$r8FSNLWRSLAibQN-NH2 896 2066.11 1034.06 1034.58 168 Ac-F$r8AYWEAc3cL$A-NH2 897 1314.70 658.35 1315.88 169 Ac-F$r8AYWEAc3cL$S-NH2 898 1330.70 666.35 1331.87 170 Ac-F$r8AYWEAc3cL$Q-NH2 899 1371.72 686.86 1372.72 171 Ac-F$r8AYWEAibL$S-NH2 900 1332.71 667.36 1334.83 172 Ac-F$r8AYWEAL$S-NH2 901 1318.70 660.35 1319.73 173 Ac-F$r8AYWEQL$S-NH2 902 1375.72 688.86 1377.53 174 Ac-F$r8HYWEQL$S-NH2 903 1441.74 721.87 1443.48 175 Ac-F$r8HYWAQL$S-NH2 904 1383.73 692.87 1385.38 176 Ac-F$r8HYWAAc3cL$S-NH2 905 1338.71 670.36 1340.82 177 Ac-F$r8HYWRAc3cL$S-NH2 906 1423.78 712.89 713.04 178 Ac-F$r8AYWEAc3cL#A-NH2 907 1300.69 651.35 1302.78 179 Ac-NlePTF%r8NYWRLL%QN-NH2 908 1899.08 950.54 950.56 180 Ac-TF$r8AAWRAL$Q-NH2 909 1395.80 698.90 699.13 181 Ac-TSF%r8HYWAQL%S-NH2 910 1573.83 787.92 787.98 184 Ac-F%r8AY6clWEAc3cL%A-NH2 911 1350.68 676.34 676.91 185 Ac-LTF$r8HYWAQI$S-NH2 912 1597.87 799.94 800.07 186 Ac-LTF$r8HYWAQNle$S-NH2 913 1597.87 799.94 800.07 187 Ac-LTF$r8HYWAQL$A-NH2 914 1581.87 791.94 792.45 188 Ac-LTF$r8HYWAQL$Abu-NH2 915 1595.89 798.95 799.03 189 Ac-LTF$r8HYWAbuQL$S-NH2 916 1611.88 806.94 807.47 190 Ac-LTFSer8AYWAQLSeS-NH2 917 1531.84 766.92 766.96 191 Ac-LAF5r8HYWAQL$S-NH2 918 1567.86 784.93 785.49 192 Ac-LAF$r8AYWAQL$S-NH2 919 1501.83 751.92 752.01 193 Ac-LTFSer8AYWAQLSeA-NH2 920 1515.85 758.93 758.97 194 Ac-LAF5r8AYWAQL$A-NH2 921 1485.84 743.92 744.05 195 Ac-LTF$r8NLWANleL$Q-NH2 922 1550.92 776.46 776.61 196 Ac-LTF$r8NLWANleL$A-NH2 923 1493.90 747.95 1495.6 197 Ac-LTF5r8ALWANleL$Q-NH2 924 1507.92 754.96 755 198 Ac-LAF$r8NLWANleL$Q-NH2 925 1520.91 761.46 761.96 199 Ac-LAF$r8ALWANleL$A-NH2 926 1420.89 711.45 1421.74 200 Ac-A$r8AYWEAc3cL$A-NH2 927 1238.67 620.34 1239.65 201 Ac-F$r8AYWEAc3cL$AA-NH2 928 1385.74 693.87 1386.64 202 Ac-F$r8AYWEAc3cL$Abu-NH2 929 1328.72 665.36 1330.17 203 Ac-F5r8AYWEAc3cL$Nle-NH2 930 1356.75 679.38 1358.22 204 Ac-F5r5AYWEAc3cL$s8A-NH2 931 1314.70 658.35 1315.51 205 Ac-FSAYWEAc3cL$r8A-NH2 932 1314.70 658.35 1315.66 206 Ac-F5r8AYWEAc3cI$A-NH2 933 1314.70 658.35 1316.18 207 Ac-F5r8AYWEAc3cNle$A-NH2 934 1314.70 658.35 1315.66 208 Ac-F$r8AYWEAmlL$A-NH2 935 1358.76 680.38 1360.21 209 Ac-F$r8AYWENleL$A-NH2 936 1344.75 673.38 1345.71 210 Ac-F$r8AYWQAc3cL$A-NH2 937 1313.72 657.86 1314.7 211 Ac-F$r8AYWAAc3cL$A-NH2 938 1256.70 629.35 1257.56 212 Ac-F$r8AYWAbuAc3cL$A-NH2 939 1270.71 636.36 1272.14 213 Ac-F$r8AYWNleAc3cL$A-NH2 940 1298.74 650.37 1299.67 214 Ac-F$r8AbuYWEAc3cL$A-NH2 941 1328.72 665.36 1329.65 215 Ac-F$r8NleYWEAc3cL$A-NH2 942 1356.75 679.38 1358.66 216 5-FAM-BaLTFEHYWAQLTS-NH2 943 1922.82 962.41 962.87 217 5-FAM-BaLTF%r8HYWAQL%S-NH2 944 1986.96 994.48 994.97 218 Ac-LTF$r8HYWAQhL$S-NH2 945 1611.88 806.94 807 219 Ac-LTF$r8HYWAQTle$S-NH2 946 1597.87 799.94 799.97 220 Ac-LTF$r8HYWAQAdm$S-NH2 947 1675.91 838.96 839.09 221 Ac-LTF$r8HYWAQhCha$S-NH2 948 1651.91 826.96 826.98 222 Ac-LTF$r8HYWAQCha$S-NH2 949 1637.90 819.95 820.02 223 Ac-LTF$r8HYWAc6cQL$S-NH2 950 1651.91 826.96 826.98 224 Ac-LTF$r8HYWAc5cQL$S-NH2 951 1637.90 819.95 820.02 225 Ac-LThF$r8HYWAQL$S-NH2 952 1611.88 806.94 807 226 Ac-LTIgI$r8HYWAQL$S-NH2 953 1625.90 813.95 812.99 227 Ac-LTF$r8HYWAQChg$S-NH2 954 1623.88 812.94 812.99 228 Ac-LTF$r8HYWAQF$S-NH2 955 1631.85 816.93 816.99 229 Ac-LTF$r8HYWAQIgl$S-NH2 956 1659.88 830.94 829.94 230 Ac-LTF$r8HYWAQCba$S-NH2 957 1609.87 805.94 805.96 231 Ac-LTF$r8HYWAQCpg$S-NH2 958 1609.87 805.94 805.96 232 Ac-LTF$r8HhYWAQL$S-NH2 959 1611.88 806.94 807 233 Ac-F$r8AYWEAc3chL$A-NH2 960 1328.72 665.36 665.43 234 Ac-F$r8AYWEAc3cTle$A-NH2 961 1314.70 658.35 1315.62 235 Ac-F$r8AYWEAc3cAdm$A-NH2 962 1392.75 697.38 697.47 236 Ac-F$r8AYWEAc3chCha$A-NH2 963 1368.75 685.38 685.34 237 Ac-F$r8AYWEAc3cCha$A-NH2 964 1354.73 678.37 678.38 238 Ac-F$r8AYWEAc6cL$A-NH2 965 1356.75 679.38 679.42 239 Ac-F$r8AYWEAc5cL$A-NH2 966 1342.73 672.37 672.46 240 Ac-hF$r8AYWEAc3cL$A-NH2 967 1328.72 665.36 665.43 241 Ac-Igl5r8AYWEAc3cL$A-NH2 968 1342.73 672.37 671.5 243 Ac-F$r8AYWEAc3cF$A-NH2 969 1348.69 675.35 675.35 244 Ac-F5r8AYWEAc3cIgl$A-NH2 970 1376.72 689.36 688.37 245 Ac-F$r8AYWEAc3cCba$A-NH2 971 1326.70 664.35 664.47 246 Ac-F$r8AYWEAc3cCpg$A-NH2 972 1326.70 664.35 664.39 247 Ac-F$r8AhYWEAc3cL$A-NH2 973 1328.72 665.36 665.43 248 Ac-F$r8AYWEAc3cL$Q-NH2 974 1371.72 686.86 1372.87 249 Ac-F$r8AYWEAibL$A-NH2 975 1316.72 659.36 1318.18 250 Ac-F$r8AYWEAL$A-NH2 976 1302.70 652.35 1303.75 251 Ac-LAF$r8AYWAAL$A-NH2 977 1428.82 715.41 715.49 252 Ac-LTF$r8HYWAAc3cL$S-NH2 978 1552.84 777.42 777.5 253 Ac-NleTF$r8HYWAQL$S-NH2 979 1597.87 799.94 800.04 254 Ac-VTF$r8HYWAQL$S-NH2 980 1583.85 792.93 793.04 255 Ac-FTF$r8HYWAQL$S-NH2 981 1631.85 816.93 817.02 256 Ac-WTF$r8HYWAQL$S-NH2 982 1670.86 836.43 836.85 257 Ac-RTF$r8HYWAQL$S-NH2 983 1640.88 821.44 821.9 258 Ac-KTF$r8HYWAQL$S-NH2 984 1612.88 807.44 807.91 259 Ac-LNleF$r8HYWAQL$S-NH2 985 1609.90 805.95 806.43 260 Ac-LVF$r8HYWAQL$S-NH2 986 1595.89 798.95 798.93 261 Ac-LFF$r8HYWAQL$S-NH2 987 1643.89 822.95 823.38 262 Ac-LWF$r8HYWAQL$S-NH2 988 1682.90 842.45 842.55 263 Ac-LRF$r8HYWAQL$S-NH2 989 1652.92 827.46 827.52 264 Ac-LKF$r8HYWAQL$S-NH2 990 1624.91 813.46 813.51 265 Ac-LTF$r8NleYWAQL$S-NH2 991 1573.89 787.95 788.05 266 Ac-LTF$r8VYWAQL$S-NH2 992 1559.88 780.94 780.98 267 Ac-LTF$r8FYWAQL$S-NH2 993 1607.88 804.94 805.32 268 Ac-LTF$r8WYWAQL$S-NH2 994 1646.89 824.45 824.86 269 Ac-LTF$r8RYWAQL$S-NH2 995 1616.91 809.46 809.51 270 Ac-LTF$r8KYWAQL$S-NH2 996 1588.90 795.45 795.48 271 Ac-LTF$r8HNleWAQL$S-NH2 997 1547.89 774.95 774.98 272 Ac-LTF$r8HVWAQL$S-NH2 998 1533.87 767.94 767.95 273 Ac-LTF$r8HFWAQL$S-NH2 999 1581.87 791.94 792.3 274 Ac-LTF$r8HWWAQL$S-NH2 1000 1620.88 811.44 811.54 275 Ac-LTF$r8HRWAQL$S-NH2 1001 1590.90 796.45 796.52 276 Ac-LTF$r8HKWAQL$S-NH2 1002 1562.90 782.45 782.53 277 Ac-LTF$r8HYWNleQL$S-NH2 1003 1639.91 820.96 820.98 278 Ac-LTF$r8HYWVQL$S-NH2 1004 1625.90 813.92 814.03 279 Ac-LTF$r8HYWFQL$S-NH2 1005 1673.90 837.95 838.03 280 Ac-LTF$r8HYWWQL$S-NH2 1006 1712.91 857.46 857.5 281 Ac-LTF$r8HYWKQL$S-NH2 1007 1654.92 828.46 828.49 282 Ac-LTF$r8HYWANleL$S-NH2 1008 1582.89 792.45 792.52 283 Ac-LTF5r8HYWAVL$S-NH2 1009 1568.88 785.44 785.49 284 Ac-LTF$r8HYWAFL$S-NH2 1010 1616.88 809.44 809.47 285 Ac-LTF$r8HYWAWL$S-NH2 1011 1655.89 828.95 829 286 Ac-LTF$r8HYWARL$S-NH2 1012 1625.91 813.96 813.98 287 Ac-LTF5r8HYWAQL$Nle-NH2 1013 1623.92 812.96 813.39 288 Ac-LTF$r8HYWAQL$V-NH2 1014 1609.90 805.95 805.99 289 Ac-LTF$r8HYWAQL$F-NH2 1015 1657.90 829.95 830.26 290 Ac-LTF$r8HYWAQL$W-NH2 1016 1696.91 849.46 849.5 291 Ac-LTF$r8HYWAQL$R-NH2 1017 1666.94 834.47 834.56 292 Ac-LTF$r8HYWAQL$K-NH2 1018 1638.93 820.47 820.49 293 Ac-Q$r8QQTFSN$WRLLAibQN-NH2 1019 2080.12 1041.06 1041.54 294 Ac-QSQQ5r8FSNLWRSLAibQN-NH2 1020 2066.11 1034.06 1034.58 295 Ac-LT2Pal$r8HYWAQL$S-NH2 1021 1598.86 800.43 800.49 296 Ac-LT3Pal$r8HYWAQL$S-NH2 1022 1598.86 800.43 800.49 297 Ac-LT4Pal$r8HYWAQL$S-NH2 1023 1598.86 800.43 800.49 298 Ac-LTF2CF3$r8HYWAQL$S-NH2 1024 1665.85 833.93 834.01 299 Ac-LTF2CN$r8HYWAQL$S-NH2 1025 1622.86 812.43 812.47 300 Ac-LTF2Me$r8HYWAQL$S-NH2 1026 1611.88 806.94 807 301 Ac-LTF3CI$r8HYWAQL$S-NH2 1027 1631.83 816.92 816.99 302 Ac-LTF4CF3Sr8HYWAQL$S-NH2 1028 1665.85 833.93 833.94 303 Ac-LTF4tBu$r8HYWAQL$S-NH2 1029 1653.93 827.97 828.02 304 Ac-LTF5F$r8HYWAQL$S-NH2 1030 1687.82 844.91 844.96 305 Ac-LTF$r8HY3BthAAQL$S-NH2 1031 1614.83 808.42 808.48 306 Ac-LTF2Br$r8HYWAQL$S-NH2 1032 1675.78 838.89 838.97 307 Ac-LTF4Br$r8HYWAQL$S-NH2 1033 1675.78 838.89 839.86 308 Ac-LTF2CI$r8HYWAQL$S-NH2 1034 1631.83 816.92 816.99 309 Ac-LTF4CI$r8HYWAQL$S-NH2 1035 1631.83 816.92 817.36 310 Ac-LTF3CN$r8HYWAQL$S-NH2 1036 1622.86 812.43 812.47 311 Ac-LTF4CN$r8HYWAQL$S-NH2 1037 1622.86 812.43 812.47 312 Ac-LTF34Cl2$r8HYWAQL$S-NH2 1038 1665.79 833.90 833.94 313 Ac-LTF34F2$r8HYWAQL$S-NH2 1039 1633.85 817.93 817.95 314 Ac-LTF35F2$r8HYWAQL$S-NH2 1040 1633.85 817.93 817.95 315 Ac-LTDip$r8HYWAQL$S-NH2 1041 1673.90 837.95 838.01 316 Ac-LTF2F$r8HYWAQL$S-NH2 1042 1615.86 808.93 809 317 Ac-LTF3F$r8HYWAQL$S-NH2 1043 1615.86 808.93 809 318 Ac-LTF4F$r8HYWAQL$S-NH2 1044 1615.86 808.93 809 319 Ac-LTF4I$r8HYWAQL$S-NH2 1045 1723.76 862.88 862.94 320 Ac-LTF3Me$r8HYWAQL$S-NH2 1046 1611.88 806.94 807.07 321 Ac-LTF4Me$r8HYWAQL$S-NH2 1047 1611.88 806.94 807 322 Ac-LT1Nal$r8HYWAQL$S-NH2 1048 1647.88 824.94 824.98 323 Ac-LT2Nal$r8HYWAQL$S-NH2 1049 1647.88 824.94 825.06 324 Ac-LTF3CF3$r8HYWAQL$S-NH2 1050 1665.85 833.93 834.01 325 Ac-LTF4NO2$r8HYWAQL$S-NH2 1051 1642.85 822.43 822.46 326 Ac-LTF3NO2$r8HYWAQL$S-NH2 1052 1642.85 822.43 822.46 327 Ac-LTF$r82ThiYWAQL$S-NH2 1053 1613.83 807.92 807.96 328 Ac-LTF$r8HBipWAQL$S-NH2 1054 1657.90 829.95 830.01 329 Ac-LTF$r8HF4tBuWAQL$S-NH2 1055 1637.93 819.97 820.02 330 Ac-LTF$r8HF4CF3WAQL$S-NH2 1056 1649.86 825.93 826.02 331 Ac-LTF$r8HF4ClWAQL$S-NH2 1057 1615.83 808.92 809.37 332 Ac-LTF$r8HF4MeWAQL$S-NH2 1058 1595.89 798.95 799.01 333 Ac-LTF$r8HF4BrWAQL$S-NH2 1059 1659.78 830.89 830.98 334 Ac-LTF$r8HF4CNWAQL$S-NH2 1060 1606.87 804.44 804.56 335 Ac-LTF$r8HF4NO2WAQL$S-NH2 1061 1626.86 814.43 814.55 336 Ac-LTF$r8H1NalWAQL$S-NH2 1062 1631.89 816.95 817.06 337 Ac-LTF$r8H2NalWAQL$S-NH2 1063 1631.89 816.95 816.99 338 Ac-LTF$r8HWAQL$S-NH2 1064 1434.80 718.40 718.49 339 Ac-LTF5r8HY1NalAQL$S-NH2 1065 1608.87 805.44 805.52 340 Ac-LTF5r8HY2NalAQL$S-NH2 1066 1608.87 805.44 805.52 341 Ac-LTF$r8HYWAQl$S-NH2 1067 1597.87 799.94 800.07 342 Ac-LTF$r8HYWAQNle$S-NH2 1068 1597.87 799.94 800.44 343 Ac-LTF$er8HYWAQL$eA-NH2 1069 1581.87 791.94 791.98 344 Ac-LTF$r8HYWAQL$Abu-NH2 1070 1595.89 798.95 799.03 345 Ac-LTF$r8HYWAbuQL$S-NH2 1071 1611.88 806.94 804.47 346 Ac-LAF5r8HYWAQL$S-NH2 1072 1567.86 784.93 785.49 347 Ac-LTF$r8NLWANleL$Q-NH2 1073 1550.92 776.46 777.5 348 Ac-LTF$r8ALWANleL$Q-NH2 1074 1507.92 754.96 755.52 349 Ac-LAF$r8NLWANleL$Q-NH2 1075 1520.91 761.46 762.48 350 Ac-F$r8AYWAAc3cL$A-NH2 1076 1256.70 629.35 1257.56 351 Ac-LTF$r8AYWAAL$S-NH2 1077 1474.82 738.41 738.55 352 Ac-LVF$r8AYWAQL$S-NH2 1078 1529.87 765.94 766 353 Ac-LTF$r8AYWAbuQL$S-NH2 1079 1545.86 773.93 773.92 354 Ac-LTF$r8AYWNleQL$S-NH2 1080 1573.89 787.95 788.17 355 Ac-LTF$r8AbuYWAQL$S-NH2 1081 1545.86 773.93 773.99 356 Ac-LTF$r8AYWHQL$S-NH2 1082 1597.87 799.94 799.97 357 Ac-LTF$r8AYWKQL$S-NH2 1083 1588.90 795.45 795.53 358 Ac-LTF5r8AYWOQL$S-NH2 1084 1574.89 788.45 788.5 359 Ac-LTF$r8AYWRQL$S-NH2 1085 1616.91 809.46 809.51 360 Ac-LTF$r8AYWSQL$S-NH2 1086 1547.84 774.92 774.96 361 Ac-LTF$r8AYWRAL$S-NH2 1087 1559.89 780.95 780.95 362 Ac-LTF$r8AYWRQL$A-NH2 1088 1600.91 801.46 801.52 363 Ac-LTF$r8AYWRAL$A-NH2 1089 1543.89 772.95 773.03 364 Ac-LTF$r5HYWAQL$s8S-NH2 1090 1597.87 799.94 799.97 365 Ac-LTF$HYWAQL$r8S-NH2 1091 1597.87 799.94 799.97 366 Ac-LTF$r8HYWAAL$S-NH2 1092 1540.84 771.42 771.48 367 Ac-LTF$r8HYWAAbuL$S-NH2 1093 1554.86 778.43 778.51 368 Ac-LTF$r8HYWALL$S-NH2 1094 1582.89 792.45 792.49 369 Ac-F$r8AYWHAL$A-NH2 1095 1310.72 656.36 656.4 370 Ac-F$r8AYWAAL$A-NH2 1096 1244.70 623.35 1245.61 371 Ac-F$r8AYWSAL$A-NH2 1097 1260.69 631.35 1261.6 372 Ac-F$r8AYWRAL$A-NH2 1098 1329.76 665.88 1330.72 373 Ac-F$r8AYWKAL$A-NH2 1099 1301.75 651.88 1302.67 374 Ac-F5r8AYWOAL$A-NH2 1100 1287.74 644.87 1289.13 375 Ac-F$r8VYWEAc3cL$A-NH2 1101 1342.73 672.37 1343.67 376 Ac-F$r8FYWEAc3cL$A-NH2 1102 1390.73 696.37 1392.14 377 Ac-F$r8WYWEAc3cL$A-NH2 1103 1429.74 715.87 1431.44 378 Ac-F$r8RYWEAc3cL$A-NH2 1104 1399.77 700.89 700.95 379 Ac-F$r8KYWEAc3cL$A-NH2 1105 1371.76 686.88 686.97 380 Ac-F$r8ANleWEAc3cL$A-NH2 1106 1264.72 633.36 1265.59 381 Ac-F$r8AVWEAc3cL$A-NH2 1107 1250.71 626.36 1252.2 382 Ac-F$r8AFWEAc3cL$A-NH2 1108 1298.71 650.36 1299.64 383 Ac-F$r8AWWEAc3cL$A-NH2 1109 1337.72 669.86 1338.64 384 Ac-F$r8ARWEAc3cL$A-NH2 1110 1307.74 654.87 655 385 Ac-F$r8AKWEAc3cL$A-NH2 1111 1279.73 640.87 641.01 386 Ac-F$r8AYWVAc3cL$A-NH2 1112 1284.73 643.37 643.38 387 Ac-F$r8AYWFAc3cL$A-NH2 1113 1332.73 667.37 667.43 388 Ac-F$r8AYWWAc3cL$A-NH2 1114 1371.74 686.87 686.97 389 Ac-F$r8AYWRAc3cL$A-NH2 1115 1341.76 671.88 671.94 390 Ac-F$r8AYWKAc3cL$A-NH2 1116 1313.75 657.88 657.88 391 Ac-F5r8AYWEVLSA-NH2 1117 1330.73 666.37 666.47 392 Ac-F$r8AYWEFL$A-NH2 1118 1378.73 690.37 690.44 393 Ac-F$r8AYWEWL$A-NH2 1119 1417.74 709.87 709.91 394 Ac-F$r8AYWERL$A-NH2 1120 1387.77 694.89 1388.66 395 Ac-F$r8AYWEKL$A-NH2 1121 1359.76 680.88 1361.21 396 Ac-F$r8AYWEAc3cL$V-NH2 1122 1342.73 672.37 1343.59 397 Ac-F$r8AYWEAc3cL$F-NH2 1123 1390.73 696.37 1392.58 398 Ac-F$r8AYWEAc3cL$W-NH2 1124 1429.74 715.87 1431.29 399 Ac-F$r8AYWEAc3cL$R-NH2 1125 1399.77 700.89 700.95 400 Ac-F$r8AYWEAc3cL$K-NH2 1126 1371.76 686.88 686.97 401 Ac-F$r8AYWEAc3cL$AV-NH2 1127 1413.77 707.89 707.91 402 Ac-F$r8AYWEAc3cL$AF-NH2 1128 1461.77 731.89 731.96 403 Ac-F$r8AYWEAc3cL$AW-NH2 1129 1500.78 751.39 751.5 404 Ac-F$r8AYWEAc3cL$AR-NH2 1130 1470.80 736.40 736.47 405 Ac-F$r8AYWEAc3cL$AK-NH2 1131 1442.80 722.40 722.41 406 Ac-F$r8AYWEAc3cL$AH-NH2 1132 1451.76 726.88 726.93 407 Ac-LTF2NO2$r8HYWAQL$S-NH2 1133 1642.85 822.43 822.54 408 Ac-LTA5r8HYAAQL$S-NH2 1134 1406.79 704.40 704.5 409 Ac-LTF$r8HYAAQL$S-NH2 1135 1482.82 742.41 742.47 410 Ac-QSQQTF5r8NLWALLSAN-NH2 1136 1966.07 984.04 984.38 411 Ac-QAibQQTF5r8NLWALLSAN-NH2 1137 1964.09 983.05 983.42 412 Ac-QAibQQTF$r8ALWALL$AN-NH2 1138 1921.08 961.54 961.59 413 Ac-AAAATF5r8AAWAALSAA-NH2 1139 1608.90 805.45 805.52 414 Ac-F$r8AAWRAL$Q-NH2 1140 1294.76 648.38 648.48 415 Ac-TF$r8AAWAAL$Q-NH2 1141 1310.74 656.37 1311.62 416 Ac-TF$r8AAWRAL$A-NH2 1142 1338.78 670.39 670.46 417 Ac-VF$r8AAWRAL$Q-NH2 1143 1393.82 697.91 697.99 418 Ac-AF$r8AAWAAL$A-NH2 1144 1223.71 612.86 1224.67 420 Ac-TF$r8AAWKAL$Q-NH2 1145 1367.80 684.90 684.97 421 Ac-TF$r8AAWOAL$Q-NH2 1146 1353.78 677.89 678.01 422 Ac-TF$r8AAWSAL$Q-NH2 1147 1326.73 664.37 664.47 423 Ac-LTF$r8AAWRAL$Q-NH2 1148 1508.89 755.45 755.49 424 Ac-F$r8AYWAQL$A-NH2 1149 1301.72 651.86 651.96 425 Ac-F5r8AWWAAL$A-NH2 1150 1267.71 634.86 634.87 426 Ac-F$r8AWWAQL$A-NH2 1151 1324.73 663.37 663.43 427 Ac-F$r8AYWEAL$-NH2 1152 1231.66 616.83 1232.93 428 Ac-F$r8AYWAAL$-NH2 1153 1173.66 587.83 1175.09 429 Ac-F$r8AYWKAL$-NH2 1154 1230.72 616.36 616.44 430 Ac-F$r8AYWOAL$-NH2 1155 1216.70 609.35 609.48 431 Ac-F$r8AYWQAL$-NH2 1156 1230.68 616.34 616.44 432 Ac-F$r8AYWAQL$-NH2 1157 1230.68 616.34 616.37 433 Ac-F$r8HYWDQL$S-NH2 1158 1427.72 714.86 714.86 434 Ac-F$r8HFWEQL$S-NH2 1159 1425.74 713.87 713.98 435 Ac-F$r8AYWHQL$S-NH2 1160 1383.73 692.87 692.96 436 Ac-F$r8AYWKQL$S-NH2 1161 1374.77 688.39 688.45 437 Ac-F5r8AYWOQL$S-NH2 1162 1360.75 681.38 681.49 438 Ac-F$r8HYWSQL$S-NH2 1163 1399.73 700.87 700.95 439 Ac-F$r8HWWEQL$S-NH2 1164 1464.76 733.38 733.44 440 Ac-F$r8HWWAQL$S-NH2 1165 1406.75 704.38 704.43 441 Ac-F$r8AWWHQL$S-NH2 1166 1406.75 704.38 704.43 442 Ac-F$r8AWWKQL$S-NH2 1167 1397.79 699.90 699.92 443 Ac-F$r8AWWOQL$S-NH2 1168 1383.77 692.89 692.96 444 Ac-F$r8HWWSQL$S-NH2 1169 1422.75 712.38 712.42 445 Ac-LTF$r8NYWANleL$Q-NH2 1170 1600.90 801.45 801.52 446 Ac-LTF$r8NLWAQL$Q-NH2 1171 1565.90 783.95 784.06 447 Ac-LTF$r8NYWANleL$A-NH2 1172 1543.88 772.94 773.03 448 Ac-LTF$r8NLWAQL$A-NH2 1173 1508.88 755.44 755.49 449 Ac-LTF$r8AYWANleL$Q-NH2 1174 1557.90 779.95 780.06 450 Ac-LTF$r8ALWAQL$Q-NH2 1175 1522.89 762.45 762.45 451 Ac-LAF$r8NYWANleL$Q-NH2 1176 1570.89 786.45 786.5 452 Ac-LAF$r8NLWAQL$Q-NH2 1177 1535.89 768.95 769.03 453 Ac-LAF5r8AYWANleL$A-NH2 1178 1470.86 736.43 736.47 454 Ac-LAF$r8ALWAQL$A-NH2 1179 1435.86 718.93 719.01 455 Ac-LAF$r8AYWAAL$A-NH2 1180 1428.82 715.41 715.41 456 Ac-F$r8AYWEAc3cL$AAib-NH2 1181 1399.75 700.88 700.95 457 Ac-F$r8AYWAQL$AA-NH2 1182 1372.75 687.38 687.78 458 Ac-F$r8AYWAAc3cL$AA-NH2 1183 1327.73 664.87 664.84 459 Ac-F$r8AYWSAc3cL$AA-NH2 1184 1343.73 672.87 672.9 460 Ac-F$r8AYWEAc3cL$AS-NH2 1185 1401.73 701.87 701.84 461 Ac-F$r8AYWEAc3cL$AT-NH2 1186 1415.75 708.88 708.87 462 Ac-F$r8AYWEAc3cL$AL-NH2 1187 1427.79 714.90 714.94 463 Ac-F$r8AYWEAc3cL$AQ-NH2 1188 1442.76 722.38 722.41 464 Ac-F$r8AFWEAc3cL$AA-NH2 1189 1369.74 685.87 685.93 465 Ac-F$r8AWWEAc3cL$AA-NH2 1190 1408.75 705.38 705.39 466 Ac-F$r8AYWEAc3cL$SA-NH2 1191 1401.73 701.87 701.99 467 Ac-F$r8AYWEAL$AA-NH2 1192 1373.74 687.87 687.93 468 Ac-F$r8AYWENleL$AA-NH2 1193 1415.79 708.90 708.94 469 Ac-F$r8AYWEAc3cL$AbuA-NH2 1194 1399.75 700.88 700.95 470 Ac-F$r8AYWEAc3cL$NleA-NH2 1195 1427.79 714.90 714.86 471 Ac-F$r8AYWEAibL$NleA-NH2 1196 1429.80 715.90 715.97 472 Ac-F$r8AYWEAL$NleA-NH2 1197 1415.79 708.90 708.94 473 Ac-F$r8AYWENleL$NleA-NH2 1198 1457.83 729.92 729.96 474 Ac-F$r8AYWEAibL$Abu-NH2 1199 1330.73 666.37 666.39 475 Ac-F$r8AYWENleL$Abu-NH2 1200 1358.76 680.38 680.39 476 Ac-F$r8AYWEAL$Abu-NH2 1201 1316.72 659.36 659.36 477 Ac-LTF$r8AFWAQL$S-NH2 1202 1515.85 758.93 759.12 478 Ac-LTF$r8AWWAQL$S-NH2 1203 1554.86 778.43 778.51 479 Ac-LTF$r8AYWAQI$S-NH2 1204 1531.84 766.92 766.96 480 Ac-LTF5r8AYWAQNle$S-NH2 1205 1531.84 766.92 766.96 481 Ac-LTF$r8AYWAQL$SA-NH2 1206 1602.88 802.44 802.48 482 Ac-LTF$r8AWWAQL$A-NH2 1207 1538.87 770.44 770.89 483 Ac-LTF$r8AYWAQI$A-NH2 1208 1515.85 758.93 759.42 484 Ac-LTF5r8AYWAQNle$A-NH2 1209 1515.85 758.93 759.42 485 Ac-LTF$r8AYWAQL$AA-NH2 1210 1586.89 794.45 794.94 486 Ac-LTF$r8HWWAQL$S-NH2 1211 1620.88 811.44 811.47 487 Ac-LTF$r8HRWAQL$S-NH2 1212 1590.90 796.45 796.52 488 Ac-LTF$r8HKWAQL$S-NH2 1213 1562.90 782.45 782.53 489 Ac-LTF$r8HYWAQL$W-NH2 1214 1696.91 849.46 849.5 491 Ac-F$r8AYWAbuAL$A-NH2 1215 1258.71 630.36 630.5 492 Ac-F$r8AbuYWEAL$A-NH2 1216 1316.72 659.36 659.51 493 Ac-NlePRF%r8NYWRLL%QN-NH2 1217 1954.13 978.07 978.54 494 Ac-TSF%r8HYWAQL%S-NH2 1218 1573.83 787.92 787.98 495 Ac-LTF%r8AYWAQL%S-NH2 1219 1533.86 767.93 768 496 Ac-HTF$r8HYWAQL$S-NH2 1220 1621.84 811.92 811.96 497 Ac-LHF$r8HYWAQL$S-NH2 1221 1633.88 817.94 818.02 498 Ac-LTF$r8HHWAQL$S-NH2 1222 1571.86 786.93 786.94 499 Ac-LTF$r8HYWHQL$S-NH2 1223 1663.89 832.95 832.38 500 Ac-LTF$r8HYWAHL$S-NH2 1224 1606.87 804.44 804.48 501 Ac-LTF$r8HYWAQL$H-NH2 1225 1647.89 824.95 824.98 502 Ac-LTF$r8HYWAQL$S-NHPr 1226 1639.91 820.96 820.98 503 Ac-LTF$r8HYWAQL$S-NHsBu 1227 1653.93 827.97 828.02 504 Ac-LTF$r8HYWAQL$S-NHiBu 1228 1653.93 827.97 828.02 505 Ac-LTF$r8HYWAQL$S-NHBn 1229 1687.91 844.96 844.44 506 Ac-LTF$r8HYWAQL$S-NHPe 1230 1700.92 851.46 851.99 507 Ac-LTF$r8HYWAQL$S-NHChx 1231 1679.94 840.97 841.04 508 Ac-ETF$r8AYWAQL$S-NH2 1232 1547.80 774.90 774.96 509 Ac-STF$r8AYWAQL$S-NH2 1233 1505.79 753.90 753.94 510 Ac-LEF$r8AYWAQL$S-NH2 1234 1559.84 780.92 781.25 511 Ac-LSF$r8AYWAQL$S-NH2 1235 1517.83 759.92 759.93 512 Ac-LTF$r8EYWAQL$S-NH2 1236 1589.85 795.93 795.97 513 Ac-LTF$r8SYWAQL$S-NH2 1237 1547.84 774.92 774.96 514 Ac-LTF$r8AYWEQL$S-NH2 1238 1589.85 795.93 795.9 515 Ac-LTF$r8AYWAEL$S-NH2 1239 1532.83 767.42 766.96 516 Ac-LTF$r8AYWASL$S-NH2 1240 1490.82 746.41 746.46 517 Ac-LTF$r8AYWAQL$E-NH2 1241 1573.85 787.93 787.98 518 Ac-LTF2CN$r8HYWAQL$S-NH2 1242 1622.86 812.43 812.47 519 Ac-LTF3CI$r8HYWAQL$S-NH2 1243 1631.83 816.92 816.99 520 Ac-LTDip$r8HYWAQL$S-NH2 1244 1673.90 837.95 838.01 521 Ac-LTF$r8HYWAQTle$S-NH2 1245 1597.87 799.94 800.04 522 Ac-F$r8AY6clWEAL$A-NH2 1246 1336.66 669.33 1338.56 523 Ac-F5r8AYdl6brWEAL$A-NH2 1247 1380.61 691.31 692.2 524 Ac-F5r8AYdl6fWEAL$A-NH2 1248 1320.69 661.35 1321.61 525 Ac-F5r8AYdl4mWEAL$A-NH2 1249 1316.72 659.36 659.36 526 Ac-F5r8AYdl5clWEAL$A-NH2 1250 1336.66 669.33 669.35 527 Ac-F5r8AYdl7mWEAL$A-NH2 1251 1316.72 659.36 659.36 528 Ac-LTF%r8HYWAQL%A-NH2 1252 1583.89 792.95 793.01 529 Ac-LTF$r8HCouWAQL$S-NH2 1253 1679.87 840.94 841.38 530 Ac-LTFEHCouWAQLTS-NH2 1254 1617.75 809.88 809.96 531 Ac-LTA5r8HCouWAQL$S-NH2 1255 1603.84 802.92 803.36 532 Ac-F$r8AYWEAL$AbuA-NH2 1256 1387.75 694.88 694.88 533 Ac-F$r8AYWEAI$AA-NH2 1257 1373.74 687.87 687.93 534 Ac-F$r8AYWEANle$AA-NH2 1258 1373.74 687.87 687.93 535 Ac-F$r8AYWEAmlL$AA-NH2 1259 1429.80 715.90 715.97 536 Ac-F5r8AYWQALSAA-NH2 1260 1372.75 687.38 687.48 537 Ac-F$r8AYWAAL$AA-NH2 1261 1315.73 658.87 658.92 538 Ac-F$r8AYWAbuAL$AA-NH2 1262 1329.75 665.88 665.95 539 Ac-F$r8AYWNleAL$AA-NH2 1263 1357.78 679.89 679.94 540 Ac-F$r8AbuYWEAL$AA-NH2 1264 1387.75 694.88 694.96 541 Ac-F$r8NleYWEAL$AA-NH2 1265 1415.79 708.90 708.94 542 Ac-F$r8FYWEAL$AA-NH2 1266 1449.77 725.89 725.97 543 Ac-LTF$r8HYWAQhL$S-NH2 1267 1611.88 806.94 807 544 Ac-LTF$r8HYWAQAdm$S-NH2 1268 1675.91 838.96 839.04 545 Ac-LTF5r8HYWAQIgl$S-NH2 1269 1659.88 830.94 829.94 546 Ac-F5r8AYWAQL$AA-NH2 1270 1372.75 687.38 687.48 547 Ac-LTF$r8ALWAQL$Q-NH2 1271 1522.89 762.45 762.52 548 Ac-F$r8AYWEAL$AA-NH2 1272 1373.74 687.87 687.93 549 Ac-F5r8AYWENleL$AA-NH2 1273 1415.79 708.90 708.94 550 Ac-F$r8AYWEAibL$Abu-NH2 1274 1330.73 666.37 666.39 551 Ac-F5r8AYWENleL$Abu-NH2 1275 1358.76 680.38 680.38 552 Ac-F$r8AYWEAL$Abu-NH2 1276 1316.72 659.36 659.36 553 Ac-F$r8AYWEAc3cL$AbuA-NH2 1277 1399.75 700.88 700.95 554 Ac-F$r8AYWEAc3cL$NleA-NH2 1278 1427.79 714.90 715.01 555 H-LTF$r8AYWAQL$S-NH2 1279 1489.83 745.92 745.95 556 mdPEG3-LTF$r8AYWAQL$S-NH2 1280 1679.92 840.96 840.97 557 mdPEG7-LTF$r8AYWAQL$S-NH2 1281 1856.02 929.01 929.03 558 Ac-F5r8AompEt6clWEAL$A-NH2 1282 1470.71 736.36 788.17 559 Ac-LTF3Cl$r8AYWAQL$S-NH2 1283 1565.81 783.91 809.18 560 Ac-LTF3Cl$r8HYWAQL$A-NH2 1284 1615.83 808.92 875.24 561 Ac-LTF3Cl$r8HYWWQL$S-NH2 1285 1746.87 874.44 841.65 562 Ac-LTF3Cl$r8AYWWQL$S-NH2 1286 1680.85 841.43 824.63 563 Ac-LTF$r8AYWWQL$S-NH2 1287 1646.89 824.45 849.98 564 Ac-LTF$r8HYWWQL$A-NH2 1288 1696.91 849.46 816.67 565 Ac-LTF$r8AYWWQL$A-NH2 1289 1630.89 816.45 776.15 566 Ac-LTF4F$r8AYWAQL$S-NH2 1290 1549.83 775.92 776.15 567 Ac-LTF2F$r8AYWAQL$S-NH2 1291 1549.83 775.92 776.15 568 Ac-LTF3F$r8AYWAQL$S-NH2 1292 1549.83 775.92 785.12 569 Ac-LTF34F2$r8AYWAQL$S-NH2 1293 1567.83 784.92 785.12 570 Ac-LTF35F2$r8AYWAQL$S-NH2 1294 1567.83 784.92 1338.74 571 Ac-F3Cl$r8AYWEAL$A-NH2 1295 1336.66 669.33 705.28 572 Ac-F3Cl$r8AYWEAL$AA-NH2 1296 1407.70 704.85 680.11 573 Ac-F5r8AY6clWEALSAA-NH2 1297 1407.70 704.85 736.83 574 Ac-F$r8AY6clWEAL$-NH2 1298 1265.63 633.82 784.1 575 Ac-LTF$r8HYWAQLSt/S-NH2 1299 16.03 9.02 826.98 576 Ac-LTF$r8HYWAQL$S-NHsBu 1300 1653.93 827.97 828.02 577 Ac-STF$r8AYWAQL$S-NH2 1301 1505.79 753.90 753.94 578 Ac-LTF$r8AYWAEL$S-NH2 1302 1532.83 767.42 767.41 579 Ac-LTF$r8AYWAQL$E-NH2 1303 1573.85 787.93 787.98 580 mdPEG3-LTF$r8AYWAQL$S-NH2 1304 1679.92 840.96 840.97 581 Ac-LTF$r8AYWAQhL$S-NH2 1305 1545.86 773.93 774.31 583 Ac-LTF$r8AYWAQCha$S-NH2 1306 1571.88 786.94 787.3 584 Ac-LTF$r8AYWAQChg$S-NH2 1307 1557.86 779.93 780.4 585 Ac-LTF$r8AYWAQCba$S-NH2 1308 1543.84 772.92 780.13 586 Ac-LTF$r8AYWAQF$S-NH2 1309 1565.83 783.92 784.2 587 Ac-LTF4F$r8HYWAQhL$S-NH2 1310 1629.87 815.94 815.36 588 Ac-LTF4F$r8HYWAQCha$S-NH2 1311 1655.89 828.95 828.39 589 Ac-LTF4F$r8HYWAQChg$S-NH2 1312 1641.87 821.94 821.35 590 Ac-LTF4F$r8HYWAQCba$S-NH2 1313 1627.86 814.93 814.32 591 Ac-LTF4F$r8AYWAQhL$S-NH2 1314 1563.85 782.93 782.36 592 Ac-LTF4F$r8AYWAQCha$S-NH2 1315 1589.87 795.94 795.38 593 Ac-LTF4F$r8AYWAQChg$S-NH2 1316 1575.85 788.93 788.35 594 Ac-LTF4F$r8AYWAQCba$S-NH2 1317 1561.83 781.92 781.39 595 Ac-LTF3Cl$r8AYWAQhL$S-NH2 1318 1579.82 790.91 790.35 596 Ac-LTF3Cl$r8AYWAQCha$S-NH2 1319 1605.84 803.92 803.67 597 Ac-LTF3Cl$r8AYWAQChg$S-NH2 1320 1591.82 796.91 796.34 598 Ac-LTF3Cl$r8AYWAQCba$S-NH2 1321 1577.81 789.91 789.39 599 Ac-LTF$r8AYWAQhF$S-NH2 1322 1579.84 790.92 791.14 600 Ac-LTF$r8AYWAQF3CF3$S-NH2 1323 1633.82 817.91 818.15 601 Ac-LTF$r8AYWAQF3Me$S-NH2 1324 1581.86 791.93 791.32 602 Ac-LTF$r8AYWAQ1Nal$S-NH2 1325 1615.84 808.92 809.18 603 Ac-LTF$r8AYWAQBip$S-NH2 1326 1641.86 821.93 822.13 604 Ac-LTF$r8FYWAQL$A-NH2 1327 1591.88 796.94 797.33 605 Ac-LTF$r8HYWAQL$S-NHAm 1328 1667.94 834.97 835.92 606 Ac-LTF$r8HYWAQL$S-NHiAm 1329 1667.94 834.97 835.55 607 Ac-LTF$r8HYWAQL$S-NHnPr3Ph 1330 1715.94 858.97 859.79 608 Ac-LTF$r8HYWAQL$S-NHnBu3,3Me 1331 1681.96 841.98 842.49 610 Ac-LTF$r8HYWAQL$S-NHnPr 1332 1639.91 820.96 821.58 611 Ac-LTF$r8HYWAQL$S-NHnEt2Ch 1333 1707.98 854.99 855.35 612 Ac-LTF$r8HYWAQL$S-NHHex 1334 1681.96 841.98 842.4 613 Ac-LTF$r8AYWAQL$S-NHmdPeg2 1335 1633.91 817.96 818.35 614 Ac-LTF$r8AYWAQL$A-NHmdPeg2 1336 1617.92 809.96 810.3 615 Ac-LTF$r8AYWAQL$A-NHmdPeg4 1337 1705.97 853.99 854.33 616 Ac-F5r8AYdl4mWEAL$A-NH2 1338 1316.72 659.36 659.44 617 Ac-F5r8AYdl5clWEAL$A-NH2 1339 1336.66 669.33 669.43 618 Ac-LThF$r8AYWAQL$S-NH2 1340 1545.86 773.93 774.11 619 Ac-LT2Nal$r8AYWAQL$S-NH2 1341 1581.86 791.93 792.43 620 Ac-LTA$r8AYWAQL$S-NH2 1342 1455.81 728.91 729.15 621 Ac-LTF$r8AYWVQL$S-NH2 1343 1559.88 780.94 781.24 622 Ac-LTF$r8HYWAAL$A-NH2 1344 1524.85 763.43 763.86 623 Ac-LTF$r8VYWAQL$A-NH2 1345 1543.88 772.94 773.37 624 Ac-LTF$r8IYWAQL$S-NH2 1346 1573.89 787.95 788.17 625 Ac-FTF$r8VYWSQL$S-NH2 1347 1609.85 805.93 806.22 626 Ac-ITF$r8FYWAQL$S-NH2 1348 1607.88 804.94 805.2 627 Ac-2NalTF$r8VYWSQL$S-NH2 1349 1659.87 830.94 831.2 628 Ac-ITF$r8LYWSQL$S-NH2 1350 1589.89 795.95 796.13 629 Ac-FTF$r8FYWAQL$S-NH2 1351 1641.86 821.93 822.13 630 Ac-WTF$r8VYWAQL$S-NH2 1352 1632.87 817.44 817.69 631 Ac-WTF$r8WYWAQL$S-NH2 1353 1719.88 860.94 861.36 632 Ac-VTF$r8AYWSQL$S-NH2 1354 1533.82 767.91 768.19 633 Ac-WTF$r8FYWSQL$S-NH2 1355 1696.87 849.44 849.7 634 Ac-FTF$r8IYWAQL$S-NH2 1356 1607.88 804.94 805.2 635 Ac-WTF$r8VYWSQL$S-NH2 1357 1648.87 825.44 824.8 636 Ac-FTF$r8LYWSQL$S-NH2 1358 1623.87 812.94 812.8 637 Ac-YTF$r8FYWSQL$S-NH2 1359 1673.85 837.93 837.8 638 Ac-LTF5r8AY6clWEAL$A-NH2 1360 1550.79 776.40 776.14 639 Ac-LTF$r8AY6clWSQL$S-NH2 1361 1581.80 791.90 791.68 640 Ac-F5r8AY6clWSAL$A-NH2 1362 1294.65 648.33 647.67 641 Ac-F5r8AY6clWQALSAA-NH2 1363 1406.72 704.36 703.84 642 Ac-LHF$r8AYWAQL$S-NH2 1364 1567.86 784.93 785.21 643 Ac-LTF$r8AYWAQL$S-NH2 1365 1531.84 766.92 767.17 644 Ac-LTF$r8AHWAQL$S-NH2 1366 1505.84 753.92 754.13 645 Ac-LTF$r8AYWAHL$S-NH2 1367 1540.84 771.42 771.61 646 Ac-LTF$r8AYWAQL$H-NH2 1368 1581.87 791.94 792.15 647 H-LTF$r8AYWAQL$A-NH2 1369 1473.84 737.92 737.29 648 Ac-HHF$r8AYWAQL$S-NH2 1370 1591.83 796.92 797.35 649 Ac-aAibWTF$r8VYWSQL$S-NH2 1371 1804.96 903.48 903.64 650 Ac-AibWTF$r8HYWAQL$S-NH2 1372 1755.91 878.96 879.4 651 Ac-AibAWTF$r8HYWAQL$S-NH2 1373 1826.95 914.48 914.7 652 Ac-fWTF$r8HYWAQL$S-NH2 1374 1817.93 909.97 910.1 653 Ac-AibWWTF$r8HYWAQL$S-NH2 1375 1941.99 972.00 972.2 654 Ac-WTF$r8LYWSQL$S-NH2 1376 1662.88 832.44 832.8 655 Ac-WTF$r8NleYWSQL$S-NH2 1377 1662.88 832.44 832.6 656 Ac-LTF$r8AYWSQL$a-NH2 1378 1531.84 766.92 767.2 657 Ac-LTF$r8EYWARL$A-NH2 1379 1601.90 801.95 802.1 658 Ac-LTF$r8EYWAHL$A-NH2 1380 1582.86 792.43 792.6 659 Ac-aTF$r8AYWAQL$S-NH2 1381 1489.80 745.90 746.08 660 Ac-AibTF$r8AYWAQL$S-NH2 1382 1503.81 752.91 753.11 661 Ac-AmfTF$r8AYWAQL$S-NH2 1383 1579.84 790.92 791.14 662 Ac-AmwTF$r8AYWAQL$S-NH2 1384 1618.86 810.43 810.66 663 Ac-NmLTF$r8AYWAQL$S-NH2 1385 1545.86 773.93 774.11 664 Ac-LNmTF$r8AYWAQL$S-NH2 1386 1545.86 773.93 774.11 665 Ac-LSarF$r8AYWAQL$S-NH2 1387 1501.83 751.92 752.18 667 Ac-LGF$r8AYWAQL$S-NH2 1388 1487.82 744.91 745.15 668 Ac-LTNmF$r8AYWAQL$S-NH2 1389 1545.86 773.93 774.2 669 Ac-TF$r8AYWAQL$S-NH2 1390 1418.76 710.38 710.64 670 Ac-ETF$r8AYWAQL$A-NH2 1391 1531.81 766.91 767.2 671 Ac-LTF$r8EYWAQL$A-NH2 1392 1573.85 787.93 788.1 672 Ac-LT2Nal$r8AYWSQL$S-NH2 1393 1597.85 799.93 800.4 673 Ac-LTF$r8AYWAAL$S-NH2 1394 1474.82 738.41 738.68 674 Ac-LTF$r8AYWAQhCha$S-NH2 1395 1585.89 793.95 794.19 675 Ac-LTF$r8AYWAQChg$S-NH2 1396 1557.86 779.93 780.97 676 Ac-LTF$r8AYWAQCba$S-NH2 1397 1543.84 772.92 773.19 677 Ac-LTF$r8AYWAQF3CF3$S-NH2 1398 1633.82 817.91 818.15 678 Ac-LTF$r8AYWAQ1Nal$S-NH2 1399 1615.84 808.92 809.18 679 Ac-LTF$r8AYWAQBip$S-NH2 1400 1641.86 821.93 822.32 680 Ac-LT2Nal$r8AYWAQL$S-NH2 1401 1581.86 791.93 792.15 681 Ac-LTF$r8AYWVQL$S-NH2 1402 1559.88 780.94 781.62 682 Ac-LTF$r8AWWAQL$S-NH2 1403 1554.86 778.43 778.65 683 Ac-FTF$r8VYWSQL$S-NH2 1404 1609.85 805.93 806.12 684 Ac-ITF$r8FYWAQL$S-NH2 1405 1607.88 804.94 805.2 685 Ac-ITF$r8LYWSQL$S-NH2 1406 1589.89 795.95 796.22 686 Ac-FTF$r8FYWAQL$S-NH2 1407 1641.86 821.93 822.41 687 Ac-VTF$r8AYWSQL$S-NH2 1408 1533.82 767.91 768.19 688 Ac-LTF$r8AHWAQL$S-NH2 1409 1505.84 753.92 754.31 689 Ac-LTF$r8AYWAQL$H-NH2 1410 1581.87 791.94 791.94 690 Ac-LTF$r8AYWAHL$S-NH2 1411 1540.84 771.42 771.61 691 Ac-aAibWTF$r8VYWSQL$S-NH2 1412 1804.96 903.48 903.9 692 Ac-AibWTF$r8HYWAQL$S-NH2 1413 1755.91 878.96 879.5 693 Ac-AibAWTF$r8HYWAQL$S-NH2 1414 1826.95 914.48 914.7 694 Ac-fWTF$r8HYWAQL$S-NH2 1415 1817.93 909.97 910.2 695 Ac-AibWWTF$r8HYWAQL$S-NH2 1416 1941.99 972.00 972.7 696 Ac-WTF$r8LYWSQL$S-NH2 1417 1662.88 832.44 832.7 697 Ac-WTF$r8NleYWSQL$S-NH2 1418 1662.88 832.44 832.7 698 Ac-LTF$r8AYWSQL$a-NH2 1419 1531.84 766.92 767.2 699 Ac-LTF$r8EYWARL$A-NH2 1420 1601.90 801.95 802.2 700 Ac-LTF$r8EYWAHL$A-NH2 1421 1582.86 792.43 792.6 701 Ac-aTF$r8AYWAQL$S-NH2 1422 1489.80 745.90 746.1 702 Ac-AibTF$r8AYWAQL$S-NH2 1423 1503.81 752.91 753.2 703 Ac-AmfTF$r8AYWAQL$S-NH2 1424 1579.84 790.92 791.2 704 Ac-AmwTF$r8AYWAQL$S-NH2 1425 1618.86 810.43 810.7 705 Ac-NmLTF$r8AYWAQL$S-NH2 1426 1545.86 773.93 774.1 706 Ac-LNmTF$r8AYWAQL$S-NH2 1427 1545.86 773.93 774.4 707 Ac-LSarF$r8AYWAQL$S-NH2 1428 1501.83 751.92 752.1 708 Ac-TF$r8AYWAQL$S-NH2 1429 1418.76 710.38 710.8 709 Ac-ETF$r8AYWAQL$A-NH2 1430 1531.81 766.91 767.4 710 Ac-LTF$r8EYWAQL$A-NH2 1431 1573.85 787.93 788.2 711 Ac-WTF$r8VYWSQL$S-NH2 1432 1648.87 825.44 825.2 713 Ac-YTF$r8FYWSQL$S-NH2 1433 1673.85 837.93 837.3 714 Ac-F5r8AY6clWSAL$A-NH2 1434 1294.65 648.33 647.74 715 Ac-ETF$r8EYWVQL$S-NH2 1435 1633.84 817.92 817.36 716 Ac-ETF$r8EHWAQL$A-NH2 1436 1563.81 782.91 782.36 717 Ac-ITF$r8EYWAQL$S-NH2 1437 1589.85 795.93 795.38 718 Ac-ITF$r8EHWVQL$A-NH2 1438 1575.88 788.94 788.42 719 Ac-ITF$r8EHWAQL$S-NH2 1439 1563.85 782.93 782.43 720 Ac-LTF4F$r8AYWAQCba$S-NH2 1440 1561.83 781.92 781.32 721 Ac-LTF3Cl$r8AYWAQhL$S-NH2 1441 1579.82 790.91 790.64 722 Ac-LTF3Cl$r8AYWAQCha$S-NH2 1442 1605.84 803.92 803.37 723 Ac-LTF3Cl$r8AYWAQChg$S-NH2 1443 1591.82 796.91 796.27 724 Ac-LTF3Cl$r8AYWAQCba$S-NH2 1444 1577.81 789.91 789.83 725 Ac-LTF$r8AY6clWSQL$S-NH2 1445 1581.80 791.90 791.75 726 Ac-LTF4F$r8HYWAQhL$S-NH2 1446 1629.87 815.94 815.36 727 Ac-LTF4F$r8HYWAQCba$S-NH2 1447 1627.86 814.93 814.32 728 Ac-LTF4F$r8AYWAQhL$S-NH2 1448 1563.85 782.93 782.36 729 Ac-LTF4F$r8AYWAQChg$S-NH2 1449 1575.85 788.93 788.35 730 Ac-ETF$r8EYWVAL$S-NH2 1450 1576.82 789.41 788.79 731 Ac-ETF$r8EHWAAL$A-NH2 1451 1506.79 754.40 754.8 732 Ac-ITF$r8EYWAAL$S-NH2 1452 1532.83 767.42 767.75 733 Ac-ITF$r8EHWVAL$A-NH2 1453 1518.86 760.43 760.81 734 Ac-ITF$r8EHWAAL$S-NH2 1454 1506.82 754.41 754.8 735 Pam-LTF$r8EYWAQL$S-NH2 1455 1786.07 894.04 894.48 736 Pam-ETF$r8EYWAQL$S-NH2 1456 1802.03 902.02 902.34 737 Ac-LTF$r8AYWLQL$S-NH2 1457 1573.89 787.95 787.39 738 Ac-LTF$r8EYWLQL$S-NH2 1458 1631.90 816.95 817.33 739 Ac-LTF$r8EHWLQL$S-NH2 1459 1605.89 803.95 804.29 740 Ac-LTF$r8VYWAQL$S-NH2 1460 1559.88 780.94 781.34 741 Ac-LTF$r8AYWSQL$S-NH2 1461 1547.84 774.92 775.33 742 Ac-ETF$r8AYWAQL$S-NH2 1462 1547.80 774.90 775.7 743 Ac-LTF$r8EYWAQL$S-NH2 1463 1589.85 795.93 796.33 744 Ac-LTF$r8HYWAQL$S-NHAm 1464 1667.94 834.97 835.37 745 Ac-LTF$r8HYWAQL$S-NHiAm 1465 1667.94 834.97 835.27 746 Ac-LTF$r8HYWAQL$S-NHnPr3Ph 1466 1715.94 858.97 859.42 747 Ac-LTF$r8HYWAQL$S-NHnBu3,3Me 1467 1681.96 841.98 842.67 748 Ac-LTF$r8HYWAQL$S-NHnBu 1468 1653.93 827.97 828.24 749 Ac-LTF$r8HYWAQL$S-NHnPr 1469 1639.91 820.96 821.31 750 Ac-LTF$r8HYWAQL$S-NHnEt2Ch 1470 1707.98 854.99 855.35 751 Ac-LTF$r8HYWAQL$S-NHHex 1471 1681.96 841.98 842.4 752 Ac-LTF$r8AYWAQL$S-NHmdPeg2 1472 1633.91 817.96 855.35 753 Ac-LTF$r8AYWAQL$A-NHmdPeg2 1473 1617.92 809.96 810.58 754 Ac-LTF5r5AYWAALSs8S-NH2 1474 1474.82 738.41 738.79 755 Ac-LTF$r8AYWCouQL$S-NH2 1475 1705.88 853.94 854.61 756 Ac-LTF$r8CouYWAQL$S-NH2 1476 1705.88 853.94 854.7 757 Ac-CouTF$r8AYWAQL$S-NH2 1477 1663.83 832.92 833.33 758 H-LTF$r8AYWAQL$A-NH2 1478 1473.84 737.92 737.29 759 Ac-HHF$r8AYWAQL$S-NH2 1479 1591.83 796.92 797.72 760 Ac-LT2Nal$r8AYWSQL$S-NH2 1480 1597.85 799.93 800.68 761 Ac-LTF$r8HCouWAQL$S-NH2 1481 1679.87 840.94 841.38 762 Ac-LTF$r8AYWCou2QL$S-NH2 1482 1789.94 895.97 896.51 763 Ac-LTF$r8Cou2YWAQL$S-NH2 1483 1789.94 895.97 896.5 764 Ac-Cou2TF$r8AYWAQL$S-NH2 1484 1747.90 874.95 875.42 765 Ac-LTF$r8ACou2WAQL$S-NH2 1485 1697.92 849.96 850.82 766 Dmaac-LTF$r8AYWAQL$S-NH2 1486 1574.89 788.45 788.82 767 Hexac-LTF$r8AYWAQL$S-NH2 1487 1587.91 794.96 795.11 768 Napac-LTF$r8AYWAQL$S-NH2 1488 1657.89 829.95 830.36 769 Pam-LTF$r8AYWAQL$S-NH2 1489 1728.06 865.03 865.45 770 Ac-LT2Nal$r8HYAAQL$S-NH2 1490 1532.84 767.42 767.61 771 Ac-LT2Nal$/r8HYWAQLS/S-NH2 1491 1675.91 838.96 839.1 772 Ac-LT2Nal$r8HYFAQL$S-NH2 1492 1608.87 805.44 805.9 773 Ac-LT2Nal$r8HWAAQL$S-NH2 1493 1555.86 778.93 779.08 774 Ac-LT2Nal$r8HYAWQL$S-NH2 1494 1647.88 824.94 825.04 775 Ac-LT2Nal$r8HYAAQW$S-NH2 1495 1605.83 803.92 804.05 776 Ac-LTW$r8HYWAQL$S-NH2 1496 1636.88 819.44 819.95 777 Ac-LT1Nal$r8HYWAQL$S-NH2 1497 1647.88 824.94 825.41

In some embodiments, a peptidomimetic macrocycles disclosed herein do not comprise a peptidomimetic macrocycle structure as shown in Table 2b.

Table 2c shows examples of non-crosslinked polypeptides comprising D-amino acids.

SEQ ID Exact Found Calc Calc Calc SP Sequence NO: Isomer Mass Mass (M + 1)/1 (M + 2)/2 (M + 3)/3 SP765 Ac-tawyanfekllr-NH2 1498 777.46 SP766 Ac-tawyanf4CF3ekllr-NH2 1499 811.41

Example 3 X-Ray Co-Crystallography of Peptidomimetic Macrocycles in Complex with MDMX

For co-crystallization with peptide 46 (Table 2b), a stoichiometric amount of compound from a 100 mM stock solution in DMSO was added to the zebrafish MDMX protein solution and allowed to sit overnight at 4° C. before setting up crystallization experiments. Procedures were similar to those described by Popowicz et al. with some variations, as noted below. Protein (residues 15-129, L46V/V95L) was obtained from an E. coli BL21(DE3) expression system using the pET15b vector. Cells were grown at 37° C. and induced with 1 mM IPTG at an OD₆₀₀ of 0.7. Cells were allowed to grow an additional 18 hr at 23° C. Protein was purified using Ni-NT Agarose followed by Superdex 75 buffered with 50 mM NaPO₄, pH 8.0, 150 mM NaCl, 2 mM TCEP and then concentrated to 24 mg/ml. The buffer was exchanged to 20 mM Tris, pH 8.0, 50 mM NaCl, 2 mM DTT for crystallization experiments. Initial crystals were obtained with the Nextal (Qiagen) AMS screen #94 and the final optimized reservoir was 2.6 M AMS, 75 mM Hepes, pH 7.5. Crystals grew routinely as thin plates at 4° C. and were cryo-protected by pulling them through a solution containing concentrated (3.4 M) malonate followed by flash cooling, storage, and shipment in liquid nitrogen.

Data collection was performed at the APS at beamline 31-ID (SGX-CAT) at 100° K and wavelength 0.97929 Å. The beamline was equipped with a Rayonix 225-HE detector. For data collection, crystals were rotated through 180° in 1° increments using 0.8 second exposure times. Data were processed and reduced using Mosflm/scala (CCP4; see The CCP4 Suite: Programs for Protein Crystallography. Acta Crystallogr. D50, 760-763 (1994); P. R. Evans. Joint CCP4 and ESF-EACBM Newsletter 33, 22-24 (1997)) in space group C2 (unit cell: a=109.2786, b=81.0836, c=30.9058 Å, α=90, β=89.8577, γ=90°). Molecular replacement with program Molrep (CCP4; seeA.Vagin & A. Teplyakov. J. Appl. Cryst. 30, 1022-1025 (1997)) was performed with the MDMX component of the structure determined by Popowicz et al. (2Z5S; see G. M. Popowicz, A. Czarna, U. Rothweiler, A. Szwagierczak, M. Krajewski, L. Weber & T. A. Holak. Cell Cycle 6, 2386-2392 (2007)) and identified two molecules in the asymmetric unit. Initial refinement of just the two molecules of the zebrafish MDMX with program Refinac (CCP4; see G. N. Murshudov, A. A. Vagin & E. J. Dodson. Acta Crystallogr. D53, 240-255 (1997)) resulted in an R-factor of 0.3424 (R_(free)=0.3712) and rmsd values for bonds (0.018 Å) and angles)(1.698°). The electron density for the stapled peptide components, starting with Gln¹⁹ and including all of the aliphatic staple, was very clear. Further refinement with CNX (Accelrys) using data to 2.3 Å resolution resulted in a model (comprised of 1448 atoms from MDMX, 272 atoms from the stapled peptides and 46 water molecules) that is well refined (R_(f)=0.2601, R_(free)=0.3162, rmsd bonds=0.007 Å and rmsd angles=0.916°).

Results from this Example are shown in FIGS. 1 and 2.

Example 4 Circular Dichroism (CD) Analysis of Alpha-Helicity

Peptide solutions were analyzed by CD spectroscopy using a Jasco J-815 spectropolarimeter (Jasco Inc., Easton, Md.) with the Jasco Spectra Manager Ver.2 system software. A Peltier temperature controller was used to maintain temperature control of the optical cell. Results are expressed as mean molar ellipticity [0] (deg cm2 dmol-1) as calculated from the equation [θ]=θobs·MRW/10*1*c where θobs is the observed ellipticity in millidegrees, MRW is the mean residue weight of the peptide (peptide molecular weight/number of residues), 1 is the optical path length of the cell in centimeters, and c is the peptide concentration in mg/ml. Peptide concentrations were determined by amino acid analysis. Stock solutions of peptides were prepared in benign CD buffer (20 mM phosphoric acid, pH 2). The stocks were used to prepare peptide solutions of 0.05 mg/ml in either benign CD buffer or CD buffer with 50% trifluoroethanol (TFE) for analyses in a 10 mm pathlength cell. Variable wavelength measurements of peptide solutions were scanned at 4° C. from 195 to 250 nm, in 0.2 nm increments, and a scan rate 50 nm per minute. The average of six scans was reported.

Table 3 shows circular dichroism data for selected peptidomimetic macrocycles:

TABLE 3 Molar Molar Molar % Helix % Helix Ellipticity Ellipticity Ellipticity 50% TFE benign Benign 50% TFE TFE-Molar compared to compared to (222 in (222 in Ellipticity 50% TFE 50% TFE SP# 0% TFE) 50% TFE) Benign parent (CD) parent (CD) 7 124 −19921.4 −20045.4 137.3 −0.9 11 −398.2 −16623.4 16225.2 106.1 2.5 41 −909 −21319.4 20410.4 136 5.8 43 −15334.5 −18247.4 2912.9 116.4 97.8 69 −102.6 −21509.7 −21407.1 148.2 0.7 71 −121.2 −17957 −17835.9 123.7 0.8 154 −916.2 −30965.1 −30048.9 213.4 6.3 230 −213.2 −17974 −17760.8 123.9 1.5 233 −477.9 −19032.6 −18554.7 131.2 3.3

Example 5 Direct Binding Assay MDM2 with Fluorescence Polarization (FP)

The assay was performed according to the following general protocol:

-   -   1. Dilute MDM2 (In-house, 41 kD) into FP buffer (High salt         buffer-200 mM Nacl, 5 mM CHAPS, pH 7.5) to make 10 μM working         stock solution.     -   2. Add 30 μl of 10 μM of protein stock solution into A1 and B1         well of 96-well black HE microplate (Molecular Devices).     -   3. Fill in 30 μl of FP buffer into column A2 to A12, B2 to B12,         C1 to C12, and D1 to D12.     -   4. 2 or 3 fold series dilution of protein stock from A1, B1 into         A2, B2; A2, B2 to A3, B3; . . . to reach the single digit nM         concentration at the last dilution point.     -   5. Dilute 1 mM (in 100% DMSO) of FAM labeled linear peptide with         DMSO to 100 μM (dilution 1:10). Then, dilute from 100 μM to 10         μM with water (dilution 1:10) and then dilute with FP buffer         from 10 μM to 40 nM (dilution 1:250). This is the working         solution which will be a 10 nM concentration in well (dilution         1:4). Keep the diluted FAM labeled peptide in the dark until         use.     -   6. Add 10 μl of 10 nM of FAM labeled peptide into each well and         incubate, and read at different time points. Kd with         5-FAM-BaLTFEHYWAQLTS-NH₂ (SEQ ID NO: 943) is ˜13.38 nM.

Example 6 Competitive Fluorescence Polarization Assay for MDM2

The assay was performed according to the following general protocol:

-   -   1. Dilute MDM2 (In-house, 41 kD) into FP buffer (High salt         buffer-200 mM Nacl, 5 mM CHAPS, pH 7.5) to make 84 nM (2×)         working stock solution.     -   2. Add 20 μl of 84 nM (2×) of protein stock solution into each         well of 96-well black HE microplate (Molecular Devices)     -   3. Dilute 1 mM (in 100% DMSO) of FAM labeled linear peptide with         DMSO to 100 μM (dilution 1:10). Then, dilute from 100 μM to 10         μM with water (dilution 1:10) and then dilute with FP buffer         from 10 μM to 40 nM (dilution 1:250). This is the working         solution which will be a 10 nM concentration in well (dilution         1:4). Keep the diluted FAM labeled peptide in the dark until         use.     -   4. Make unlabeled peptide dose plate with FP buffer starting         with 1 μM (final) of peptide and making 5 fold serial dilutions         for 6 points using following dilution scheme.     -    Dilute 10 mM (in 100% DMSO) with DMSO to 5 mM (dilution 1:2).         Then, dilute from 5 mM to 500 μM with H₂O (dilution 1:10) and         then dilute with FP buffer from 500 μM to 20 μM (dilution 1:25).         Making 5 fold serial dilutions from 4 μM (4×) for 6 points.     -   5. Transfer 10 μl of serial diluted unlabeled peptides to each         well which is filled with 20 μl of 84 nM of protein.     -   6. Add 14.1 of 10 nM (4×) of FAM labeled peptide into each well         and incubate for 3 hr to read.

Example 7 Direct Binding Assay MDMX with Fluorescence Polarization (FP)

The assay was performed according to the following general protocol:

-   -   1. Dilute MDMX (In-house, 40 kD) into FP buffer (High salt         buffer-200 mM Nacl, 5 mM CHAPS, pH 7.5) to make 10 μM working         stock solution.     -   2. Add 30 λl of 10 μM of protein stock solution into A1 and B1         well of 96-well black HE microplate (Molecular Devices).     -   3. Fill in 30 μl of FP buffer into column A2 to A12, B2 to B12,         C1 to C12, and D1 to D12.     -   4. 2 or 3 fold series dilution of protein stock from A1, B1 into         A2, B2; A2, B2 to A3, B3; . . . to reach the single digit nM         concentration at the last dilution point.     -   5. Dilute 1 mM (in 100% DMSO) of FAM labeled linear peptide with         DMSO to 100 μM (dilution 1:10). Then, dilute from 100 μM to 10         μM with water (dilution 1:10) and then dilute with FP buffer         from 10 μM to 40 nM (dilution 1:250). This is the working         solution which will be a 10 nM concentration in well (dilution         1:4). Keep the diluted FAM labeled peptide in the dark until         use.     -   6. Add 10 μl of 10 nM of FAM labeled peptide into each well and         incubate, and read at different time points.     -    Kd with 5-FAM-BaLTFEHYWAQLTS-NH₂ (SEQ ID NO: 943) is ˜51 nM.

Example 8 Competitive Fluorescence Polarization Assay for MDMX

The assay was performed according to the following general protocol:

-   -   1. Dilute MDMX (In-house, 40 kD) into FP buffer (High salt         buffer-200 mM Nacl, 5 mM CHAPS, pH 7.5.) to make 300 nM (2×)         working stock solution.     -   2. Add 20 μl of 300 nM (2×) of protein stock solution into each         well of 96-well black HE microplate (Molecular Devices)     -   3. Dilute 1 mM (in 100% DMSO) of FAM labeled linear peptide with         DMSO to 100 μM (dilution 1:10). Then, dilute from 100 μM to 10         μM with water (dilution 1:10) and then dilute with FP buffer         from 10 μM to 40 nM (dilution 1:250). This is the working         solution which will be a 10 nM concentration in well (dilution         1:4). Keep the diluted FAM labeled peptide in the dark until         use.     -   4. Make unlabeled peptide dose plate with FP buffer starting         with 5 μM (final) of peptide and making 5 fold serial dilutions         for 6 points using following dilution scheme.     -   5. Dilute 10 mM (in 100% DMSO) with DMSO to 5 mM (dilution 1:2).         Then, dilute from 5 mM to 500 μM with H₂O (dilution 1:10) and         then dilute with FP buffer from 500 μM to 20 μM (dilution 1:25).         Making 5 fold serial dilutions from 20 μM (4×) for 6 points.     -   6. Transfer 10 μl of serial diluted unlabeled peptides to each         well which is filled with 20 μl of 300 nM of protein.     -   7. Add 10 μl of 10 nM (4×) of FAM labeled peptide into each well         and incubate for 3 hr to read. Results from Examples 5-8 are         shown in Table 4. The following scale is used: “+” represents a         value greater than 1000 nM, “++” represents a value greater than         100 and less than or equal to 1000 nM, “+++” represents a value         greater than 10 nM and less than or equal to 100 nM, and “++++”         represents a value of less than or equal to 10 nM.

TABLE 4 SP# IC50 (MDM2) IC50 (MDMX) Ki (MDM2) Ki (MDMX) 3 ++ ++ +++ +++ 4 +++ ++ ++++ +++ 5 +++ ++ ++++ +++ 6 ++ ++ +++ +++ 7 +++ +++ ++++ +++ 8 ++ ++ +++ +++ 9 ++ ++ +++ +++ 10 ++ ++ +++ +++ 11 +++ ++ ++++ +++ 12 + + +++ ++ 13 ++ ++ +++ ++ 14 +++ +++ ++++ ++++ 15 +++ ++ +++ +++ 16 +++ +++ ++++ +++ 17 +++ +++ ++++ +++ 18 +++ +++ ++++ ++++ 19 ++ +++ +++ +++ 20 ++ ++ +++ +++ 21 ++ +++ +++ +++ 22 +++ +++ ++++ +++ 23 ++ ++ +++ +++ 24 +++ ++ ++++ +++ 26 +++ ++ ++++ +++ 28 +++ +++ ++++ +++ 30 ++ ++ +++ +++ 32 +++ ++ ++++ +++ 38 + ++ ++ +++ 39 + ++ ++ ++ 40 ++ ++ ++ +++ 41 ++ +++ +++ +++ 42 ++ ++ +++ ++ 43 +++ +++ ++++ +++ 45 +++ +++ ++++ ++++ 46 +++ +++ ++++ +++ 47 ++ ++ +++ +++ 48 ++ ++ +++ +++ 49 ++ ++ +++ +++ 50 +++ ++ ++++ +++ 52 +++ +++ ++++ ++++ 54 ++ ++ +++ +++ 55 + + ++ ++ 65 +++ ++ ++++ +++ 68 ++ ++ +++ +++ 69 +++ ++ ++++ +++ 70 ++ ++ ++++ +++ 71 +++ ++ ++++ +++ 75 +++ ++ ++++ +++ 77 +++ ++ ++++ +++ 80 +++ ++ ++++ +++ 81 ++ ++ +++ +++ 82 ++ ++ +++ +++ 85 +++ ++ ++++ +++ 99 ++++ ++ ++++ +++ 100 ++ ++ ++++ +++ 101 +++ ++ ++++ +++ 102 ++ ++ ++++ +++ 103 ++ ++ ++++ +++ 104 +++ ++ ++++ +++ 105 +++ ++ ++++ +++ 106 ++ ++ +++ +++ 107 ++ ++ +++ +++ 108 +++ ++ ++++ +++ 109 +++ ++ ++++ +++ 110 ++ ++ ++++ +++ 111 ++ ++ ++++ +++ 112 ++ ++ +++ +++ 113 ++ ++ +++ +++ 114 +++ ++ ++++ +++ 115 ++++ ++ ++++ +++ 116 + + ++ ++ 118 ++++ ++ ++++ +++ 120 +++ ++ ++++ +++ 121 ++++ ++ ++++ +++ 122 ++++ ++ ++++ +++ 123 ++++ ++ ++++ +++ 124 ++++ ++ ++++ +++ 125 ++++ ++ ++++ +++ 126 ++++ ++ ++++ +++ 127 ++++ ++ ++++ +++ 128 ++++ ++ ++++ +++ 129 ++++ ++ ++++ +++ 130 ++++ ++ ++++ +++ 133 ++++ ++ ++++ +++ 134 ++++ ++ ++++ +++ 135 ++++ ++ ++++ +++ 136 ++++ ++ ++++ +++ 137 ++++ ++ ++++ +++ 139 ++++ ++ ++++ +++ 142 ++++ +++ ++++ +++ 144 ++++ ++ ++++ +++ 146 ++++ ++ ++++ +++ 148 ++++ ++ ++++ +++ 150 ++++ ++ ++++ +++ 153 ++++ +++ ++++ +++ 154 ++++ +++ ++++ ++++ 156 ++++ ++ ++++ +++ 158 ++++ ++ ++++ +++ 160 ++++ ++ ++++ +++ 161 ++++ ++ ++++ +++ 166 ++++ ++ ++++ +++ 167 +++ ++ ++++ ++ 169 ++++ +++ ++++ +++ 170 ++++ ++ ++++ +++ 173 ++++ ++ ++++ +++ 175 ++++ ++ ++++ +++ 177 +++ ++ ++++ +++ 180 +++ ++ ++++ +++ 182 ++++ ++ ++++ +++ 185 +++ + ++++ ++ 186 +++ ++ ++++ +++ 189 +++ ++ ++++ +++ 192 +++ ++ ++++ +++ 194 +++ ++ ++++ ++ 196 +++ ++ ++++ +++ 197 ++++ ++ ++++ +++ 199 +++ ++ ++++ ++ 201 +++ ++ ++++ ++ 203 +++ ++ ++++ +++ 204 +++ ++ ++++ +++ 206 +++ ++ ++++ +++ 207 ++++ ++ ++++ +++ 210 ++++ ++ ++++ +++ 211 ++++ ++ ++++ +++ 213 ++++ ++ ++++ +++ 215 +++ ++ ++++ +++ 217 ++++ ++ ++++ +++ 218 ++++ ++ ++++ +++ 221 ++++ +++ ++++ +++ 227 ++++ ++ ++++ +++ 230 ++++ +++ ++++ ++++ 232 ++++ ++ ++++ +++ 233 ++++ +++ ++++ +++ 236 +++ ++ ++++ +++ 237 +++ ++ ++++ +++ 238 +++ +++ ++++ +++ 239 +++ ++ +++ +++ 240 +++ ++ ++++ +++ 241 +++ ++ ++++ +++ 242 +++ ++ ++++ +++ 243 +++ +++ ++++ +++ 244 +++ +++ ++++ ++++ 245 +++ +++ ++++ +++ 246 +++ ++ ++++ +++ 247 +++ +++ ++++ +++ 248 +++ +++ ++++ +++ 249 +++ +++ ++++ ++++ 250 ++ + ++ + 252 ++ + ++ + 254 +++ ++ ++++ +++ 255 +++ +++ ++++ +++ 256 +++ +++ ++++ +++ 257 +++ +++ ++++ +++ 258 +++ ++ ++++ +++ 259 +++ +++ ++++ +++ 260 +++ +++ ++++ +++ 261 +++ ++ ++++ +++ 262 +++ ++ ++++ +++ 263 +++ ++ ++++ +++ 264 +++ +++ ++++ +++ 266 +++ ++ ++++ +++ 267 +++ +++ ++++ ++++ 270 ++++ +++ ++++ +++ 271 ++++ +++ ++++ ++++ 272 ++++ +++ ++++ ++++ 276 +++ +++ ++++ ++++ 277 +++ +++ ++++ ++++ 278 +++ +++ ++++ ++++ 279 ++++ +++ ++++ +++ 280 +++ ++ ++++ +++ 281 +++ + +++ ++ 282 ++ + +++ + 283 +++ ++ +++ ++ 284 +++ ++ ++++ +++ 289 +++ +++ ++++ +++ 291 +++ +++ ++++ ++++ 293 ++++ +++ ++++ +++ 306 ++++ ++ ++++ +++ 308 ++ ++ +++ +++ 310 +++ +++ ++++ +++ 312 +++ ++ +++ +++ 313 ++++ ++ ++++ +++ 314 ++++ +++ ++++ ++++ 315 +++ +++ ++++ +++ 316 ++++ ++ ++++ +++ 317 +++ ++ +++ +++ 318 +++ ++ +++ +++ 319 +++ ++ +++ ++ 320 +++ ++ +++ ++ 321 +++ ++ ++++ +++ 322 +++ ++ +++ ++ 323 +++ + +++ ++ 328 +++ +++ ++++ +++ 329 +++ +++ ++++ +++ 331 ++++ +++ ++++ ++++ 332 ++++ +++ ++++ ++++ 334 ++++ +++ ++++ ++++ 336 ++++ +++ ++++ ++++ 339 ++++ ++ ++++ +++ 341 +++ +++ ++++ ++++ 343 +++ +++ ++++ ++++ 347 +++ +++ ++++ +++ 349 ++++ +++ ++++ ++++ 351 ++++ +++ ++++ ++++ 353 ++++ +++ ++++ ++++ 355 ++++ +++ ++++ ++++ 357 ++++ +++ ++++ ++++ 359 ++++ +++ ++++ +++ 360 ++++ ++++ ++++ ++++ 363 +++ +++ ++++ ++++ 364 +++ +++ ++++ ++++ 365 +++ +++ ++++ ++++ 366 +++ +++ ++++ +++ 369 ++ ++ +++ +++ 370 +++ +++ ++++ +++ 371 ++ ++ +++ +++ 372 ++ ++ +++ +++ 373 +++ +++ +++ +++ 374 +++ +++ ++++ ++++ 375 +++ +++ ++++ ++++ 376 +++ +++ ++++ ++++ 377 +++ +++ ++++ +++ 378 +++ +++ ++++ +++ 379 +++ +++ ++++ +++ 380 +++ +++ ++++ +++ 381 +++ +++ ++++ +++ 382 +++ +++ ++++ ++++ 384 ++ + ++ + 386 ++ + ++ + 388 ++ +++ +++ ++++ 390 +++ +++ ++++ +++ 392 +++ +++ ++++ ++++ 394 ++++ +++ ++++ ++++ 396 ++++ ++++ ++++ ++++ 398 +++ +++ ++++ +++ 402 ++++ ++++ ++++ ++++ 404 +++ +++ ++++ ++++ 408 +++ +++ ++++ +++ 410 ++++ ++++ ++++ ++++ 411 ++ + ++ + 412 ++++ +++ ++++ ++++ 415 ++++ ++++ ++++ ++++ 416 +++ +++ ++++ +++ 417 +++ +++ ++++ +++ 418 ++++ +++ ++++ ++++ 419 +++ +++ +++ ++++ 421 ++++ ++++ ++++ ++++ 423 +++ +++ ++++ +++ 425 +++ +++ +++ +++ 427 ++ ++ +++ +++ 432 ++++ +++ ++++ ++++ 434 +++ +++ ++++ +++ 435 ++++ +++ ++++ ++++ 437 +++ +++ ++++ +++ 439 ++++ +++ ++++ ++++ 441 ++++ ++++ ++++ ++++ 443 +++ +++ ++++ +++ 445 +++ ++ ++++ +++ 446 +++ + ++++ + 447 ++ + ++ + 551 N/A N/A ++++ +++ 555 N/A N/A ++++ +++ 556 N/A N/A ++++ +++ 557 N/A N/A +++ +++ 558 N/A N/A +++ +++ 559 N/A N/A +++ +++ 560 N/A N/A + + 561 N/A N/A ++++ +++ 562 N/A N/A +++ +++ 563 N/A N/A +++ +++ 564 N/A N/A ++++ +++ 565 N/A N/A +++ +++ 566 N/A N/A ++++ +++ 567 N/A N/A ++++ +++ 568 N/A N/A ++++ ++++ 569 N/A N/A ++++ +++ 570 N/A N/A ++++ +++ 571 N/A N/A ++++ +++ 572 N/A N/A +++ +++ 573 N/A N/A +++ +++ 574 N/A N/A ++++ +++ 575 N/A N/A ++++ +++ 576 N/A N/A ++++ +++ 577 N/A N/A ++++ +++ 578 N/A N/A ++++ +++ 585 N/A N/A +++ +++ 586 N/A N/A ++++ +++ 587 N/A N/A ++++ ++++ 589 N/A N/A ++++ 594 N/A N/A ++++ ++++ 596 N/A N/A ++++ +++ 597 N/A N/A ++++ +++ 598 N/A N/A ++++ +++ 600 N/A N/A ++++ ++++ 602 N/A N/A ++++ ++++ 603 N/A N/A ++++ ++++ 604 N/A N/A +++ +++ 608 N/A N/A ++++ +++ 609 N/A N/A ++++ +++ 610 N/A N/A ++++ +++ 611 N/A N/A ++++ +++ 612 N/A N/A ++++ +++ 613 N/A N/A ++++ +++ 615 N/A N/A ++++ ++++ 433 N/A N/A ++++ +++ 686 N/A N/A ++++ +++ 687 N/A N/A ++ ++ 595 N/A N/A + N/A 665 N/A N/A +++ N/A 708 N/A N/A +++ +++ 710 N/A N/A +++ +++ 711 N/A N/A +++ ++ 712 N/A N/A ++++ ++++ 713 N/A N/A ++++ ++++ 716 N/A N/A ++++ ++++ 765 + + 766 +++ + 752 ++ + 753 +++ + 754 ++ + 755 ++++ + 756 +++ + 757 ++++ + 758 +++ +

Example 9 Competition Binding ELISA (MDM2 & MDMX)

p53-His6 protein (“His6” disclosed as SEQ ID NO: 1501) (30 nM/well) is coated overnight at room temperature in the wells of a 96-well Immulon plates. On the day of the experiment, plates are washed with 1×PBS-Tween 20 (0.05%) using an automated ELISA plate washer, blocked with ELISA Micro well Blocking for 30 minutes at room temperature; excess blocking agent is washed off by washing plates with 1×PBS-Tween 20 (0.05%). Peptides are diluted from 10 mM DMSO stocks to 500 μM working stocks in sterile water, further dilutions made in 0.5% DMSO to keep the concentration of DMSO constant across the samples. The peptides are added to wells at 2× desired concentrations in 50 μl volumes, followed by addition of diluted GST-MDM2 or GST-HMDX protein (final concentration: 10 nM). Samples are incubated at room temperature for 2 h, plates are washed with PBS-Tween 20 (0.05%) prior to adding 100 μl of HRP-conjugated anti-GST antibody [Hypromatrix, INC] diluted to 0.5 μg/ml in HRP-stabilizing buffer. Post 30 min incubation with detection antibody, plates are washed and incubated with 100 μl per well of TMB-E Substrate solution up to 30 minutes; reactions are stopped using 1M HCL and absorbance measured at 450 nm on micro plate reader. Data is analyzed using Graph Pad PRISM software.

Example 10 Cell Viability Assay

The assay was performed according to the following general protocol:

Cell Plating Trypsinize, count and seed cells at the pre-determined densities in 96-well plates a day prior to assay. Following cell densities are used for each cell line in use:

-   -   SJSA-1: 7500 cells/well     -   RKO: 5000 cells/well     -   RKO-E6: 5000 cells/well     -   HCT-116: 5000 cells/well     -   SW-480: 2000 cells/well     -   MCF-7: 5000 cells/well

On the day of study, replace media with fresh media with 11% FBS (assay media) at room temperature. Add 180 μL of the assay media per well. Control wells with no cells, receive 200 μl media.

Peptide dilution: all dilutions are made at room temperature and added to cells at room temperature.

-   -   Prepare 10 mM stocks of the peptides in DMSO. Serially dilute         the stock using 1:3 dilution scheme to get 10, 3.3, 1.1, 0.33,         0.11, 0.03, 0.01 mM solutions using DMSO as diluents. Dilute the         serially DMSO-diluted peptides 33.3 times using sterile water.         This gives range of 10× working stocks. Also prepare         DMSO/sterile water (3% DMSO) mix for control wells.     -   Thus the working stocks concentration range μM will be 300, 100,         30, 10, 3, 1, 0.3 and 0 μM. Mix well at each dilution step using         multichannel     -   Row H has controls. H1-H3 will receive 20 ul of assay media.         H4-H9 will receive 20 ul of 3% DMSO-water vehicle. H10-H12 will         have media alone control with no cells.     -   Positive control: MDM2 small molecule inhibitor, Nutlin-3a (10         mM) is used as positive control. Nutlin was diluted using the         same dilution scheme as peptides.

Addition of working stocks to cells:

-   -   Add 20 μl of 10× desired concentration to appropriate well to         achieve the final concentrations in total 200 μl volume in well.         (20 μl of 300 μM peptide +180 μl of cells in media=30 μM final         concentration in 200 μl volume in wells). Mix gently a few times         using pipette. Thus final concentration range used will be 30,         10, 3, 1, 0.3, 0.1, 0.03 & 0 μM (for potent peptides further         dilutions are included).     -   Controls include wells that get no peptides but contain the same         concentration of DMSO as the wells containing the peptides, and         wells containing NO CELLS.     -   Incubate for 72 hours at 37° C. in humidified 5% CO₂ atmosphere.     -   The viability of cells is determined using MTT reagent from         Promega. Viability of SJSA-1, RKO, RKO-E6, HCT-116 cells is         determined on day 3, MCF-7 cells on day 5 and SW-480 cells on         day 6. At the end of designated incubation time, allow the         plates to come to room temperature. Remove 80 μl of assay media         from each well. Add 15 μl of thawed MTT reagent to each well.     -   Allow plate to incubate for 2 h at 37° C. in humidified 5% CO₂         atmosphere and add 100 μl solubilization reagent as per         manufacturer's protocol. Incubate with agitation for 1 h at room         temperature and read on Synergy Biotek multiplate reader for         absorbance at 570 nM.     -   Analyze the cell viability against the DMSO controls using         GraphPad PRISM analysis tools.

Reagents:

-   -   Invitrogen cell culture Media         -   i. Falcon 96-well clear cell culture treated plates (Nunc             353072)     -   DMSO (Sigma D 2650)     -   RPMI 1640 (Invitrogen 72400)     -   MTT (Promega G4000)

Instruments:

Multiplate Reader for Absorbance readout (Synergy 2). Results from cell viability assays are shown in Tables 5 and 6. The following scale is used: “+” represents a value greater than 30 μM, “++” represents a value greater than 15 μM and less than or equal to 30 μM, “+++” represents a value greater than 5 μM and less than or equal to 15 μM, and “++++” represents a value of less than or equal to 5 μM. “IC50 ratio” represents the ratio of average IC50 in p53+/+ cells relative to average IC50 in p53−/− cells.

TABLE 5 SP# SJSA-1 EC50 (72 h) 3 +++ 4 +++ 5 ++++ 6 ++ 7 ++++ 8 +++ 9 +++ 10 +++ 11 ++++ 12 ++ 13 +++ 14 + 15 ++ 16 + 17 + 18 + 19 ++ 20 + 21 + 22 + 24 +++ 26 ++++ 28 + 29 + 30 + 32 ++ 38 + 39 + 40 + 41 + 42 + 43 ++ 45 + 46 + 47 + 48 + 49 +++ 50 ++++ 52 + 54 + 55 + 65 ++++ 68 ++++ 69 ++++ 70 ++++ 71 ++++ 72 ++++ 74 ++++ 75 ++++ 77 ++++ 78 ++ 80 ++++ 81 +++ 82 +++ 83 +++ 84 + 85 +++ 99 ++++ 102 +++ 103 +++ 104 +++ 105 +++ 108 +++ 109 +++ 110 +++ 111 ++ 114 ++++ 115 ++++ 118 ++++ 120 ++++ 121 ++++ 122 ++++ 123 ++++ 124 +++ 125 ++++ 126 ++++ 127 ++++ 128 +++ 129 ++ 130 ++++ 131 +++ 132 ++++ 133 +++ 134 +++ 135 +++ 136 ++ 137 +++ 139 ++++ 142 +++ 144 ++++ 147 ++++ 148 ++++ 149 ++++ 150 ++++ 152 +++ 153 ++++ 154 ++++ 155 ++ 156 +++ 157 +++ 158 +++ 160 ++++ 161 ++++ 162 +++ 163 +++ 166 ++ 167 +++ 168 ++ 169 ++++ 170 ++++ 171 ++ 173 +++ 174 ++++ 175 +++ 176 +++ 177 ++++ 179 +++ 180 +++ 181 +++ 182 ++++ 183 ++++ 184 +++ 185 +++ 186 ++ 188 ++ 190 ++++ 192 +++ 193 ++ 194 + 195 ++++ 196 ++++ 197 ++++ 198 ++ 199 +++ 200 +++ 201 ++++ 202 +++ 203 ++++ 204 ++++ 205 ++ 206 ++ 207 +++ 208 +++ 209 ++++ 210 +++ 211 ++++ 213 ++++ 214 ++++ 215 ++++ 216 ++++ 217 ++++ 218 ++++ 219 ++++ 220 +++ 221 ++++ 222 +++ 223 ++++ 224 ++ 225 +++ 226 ++ 227 +++ 228 ++++ 229 ++++ 230 ++++ 231 ++++ 232 ++++ 233 ++++ 234 ++++ 235 ++++ 236 ++++ 237 ++++ 238 ++++ 239 +++ 240 ++ 241 +++ 242 ++++ 243 ++++ 244 ++++ 245 ++++ 246 +++ 247 ++++ 248 ++++ 249 ++++ 250 ++ 251 + 252 + 253 + 254 +++ 255 +++ 256 ++ 257 +++ 258 +++ 259 ++ 260 ++ 261 ++ 262 +++ 263 ++ 264 ++++ 266 +++ 267 ++++ 270 ++ 271 ++ 272 ++ 276 ++ 277 ++ 278 ++ 279 ++++ 280 +++ 281 ++ 282 ++ 283 ++ 284 ++++ 289 ++++ 290 +++ 291 ++++ 292 ++++ 293 ++++ 294 ++++ 295 +++ 296 ++++ 297 +++ 298 ++++ 300 ++++ 301 ++++ 302 ++++ 303 ++++ 304 ++++ 305 ++++ 306 ++++ 307 +++ 308 ++++ 309 +++ 310 ++++ 312 ++++ 313 ++++ 314 ++++ 315 ++++ 316 ++++ 317 ++++ 318 ++++ 319 ++++ 320 ++++ 321 ++++ 322 ++++ 323 ++++ 324 ++++ 326 ++++ 327 ++++ 328 ++++ 329 ++++ 330 ++++ 331 ++++ 332 ++++ 333 ++ 334 +++ 335 ++++ 336 ++++ 337 ++++ 338 ++++ 339 ++++ 340 ++++ 341 ++++ 342 ++++ 343 ++++ 344 ++++ 345 ++++ 346 ++++ 347 ++++ 348 ++++ 349 ++++ 350 ++++ 351 ++++ 352 ++++ 353 ++++ 355 ++++ 357 ++++ 358 ++++ 359 ++++ 360 ++++ 361 +++ 362 ++++ 363 ++++ 364 ++++ 365 +++ 366 ++++ 367 ++++ 368 + 369 ++++ 370 ++++ 371 ++++ 372 +++ 373 +++ 374 ++++ 375 ++++ 376 ++++ 377 ++++ 378 ++++ 379 ++++ 380 ++++ 381 ++++ 382 ++++ 386 +++ 388 ++ 390 ++++ 392 +++ 394 +++ 396 +++ 398 +++ 402 +++ 404 +++ 408 ++++ 410 +++ 411 +++ 412 + 421 +++ 423 ++++ 425 ++++ 427 ++++ 434 +++ 435 ++++ 436 ++++ 437 ++++ 438 ++++ 439 ++++ 440 ++++ 441 ++++ 442 ++++ 443 ++++ 444 +++ 445 ++++ 449 ++++ 551 ++++ 552 ++++ 554 + 555 ++++ 557 ++++ 558 ++++ 560 + 561 ++++ 562 ++++ 563 ++++ 564 ++++ 566 ++++ 567 ++++ 568 +++ 569 ++++ 571 ++++ 572 ++++ 573 ++++ 574 ++++ 575 ++++ 576 ++++ 577 ++++ 578 ++++ 585 ++++ 586 ++++ 587 ++++ 588 ++++ 589 +++ 432 ++++ 672 + 673 ++ 682 + 686 + 687 + 662 ++++ 663 ++++ 553 +++ 559 ++++ 579 ++++ 581 ++++ 582 ++ 582 ++++ 584 +++ 675 ++++ 676 ++++ 677 + 679 ++++ 700 +++ 704 +++ 591 + 706 ++ 695 ++ 595 ++++ 596 ++++ 597 +++ 598 +++ 599 ++++ 600 ++++ 601 +++ 602 +++ 603 +++ 604 +++ 606 ++++ 607 ++++ 608 ++++ 610 ++++ 611 ++++ 612 ++++ 613 +++ 614 +++ 615 ++++ 618 ++++ 619 ++++ 707 ++++ 620 ++++ 621 ++++ 622 ++++ 623 ++++ 624 ++++ 625 ++++ 626 +++ 631 ++++ 633 ++++ 634 ++++ 635 +++ 636 +++ 638 + 641 +++ 665 ++++ 708 ++++ 709 +++ 710 + 711 ++++ 712 ++++ 713 ++++ 714 +++ 715 +++ 716 ++++ 765 + 753 + 754 + 755 + 756 + 757 ++++ 758 +++

TABLE 6 HCT-116 RKO RKO-E6 SW480 EC50 EC50 EC50 EC50 IC50 SP# (72 h) (72 h) (72 h) (6 days) Ratio 4 ++++ ++++ +++ ++++ 5 ++++ ++++ +++ ++++ 7 ++++ ++++ +++ ++++ 10 ++++ +++ +++ +++ 11 ++++ ++++ ++ +++ 50 ++++ ++++ ++ +++ 65 +++ +++ +++ +++ 69 ++++ ++++ + ++++ 70 ++++ ++++ ++ +++ 71 ++++ ++++ +++ +++ 81 +++ +++ +++ +++ 99 ++++ ++++ +++ ++++ 109 ++++ ++++ ++ +++ 114 +++ + +++ 115 +++ + +++  1-29 118 +++ ++++ + ++++ 120 ++++ ++++ + ++++ 121 ++++ ++++ + ++++ 122 +++ + +++  1-29 125 +++ +++ + + 126 + + + + 148 ++ + + 150 ++ + + 153 +++ + 154 +++ +++ + + 30-49 158 + + + + 160 +++ + + +  1-29 161 +++ + + + 175 + + + + 196 ++++ ++++ +++ ++++ 219 ++++ +++ + +  1-29 233 ++++ 237 ++++ + + 238 ++++ + + 243 ++++ + + 244 ++++ + + ≧50 245 ++++ + + 247 ++++ + + 249 ++++ ++++ + + ≧50 255 ++++ + 291 + 293 +++ + 303 +++ +  1-29 305 + 306 ++++ + 310 ++++ + 312 ++++ 313 ++++ ++ 314 + 315 ++++ ++++ ++ ++++ ≧50 316 ++++ ++++ + +++ ≧50 317 +++ + ++ 321 ++++ + 324 +++ + 325 +++ 326 +++ + 327 +++ + 328 +++ ++ 329 ++++ + 330 + 331 ++++ ++++ + + ≧50 338 ++++ ++++ ++ +++ 341 +++ ++ + + 343 +++ + + 346 ++++ + + 347 +++ + + 349 ++++ +++ + + 30-49 350 ++++ + + 351 ++++ +++ + + 30-49 353 ++ ++ + + 355 ++++ ++ + +  1-29 357 ++++ ++++ + + 358 ++++ ++ + + 359 ++++ ++ + + 367 ++++ + + 30-49 386 ++++ ++++ ++++ ++++ 388 ++ ++ + +++  1-29 390 ++++ ++++ +++ ++++ 435 +++ ++ + 436 ++++ ++++ ++ 437 ++++ ++++ ++ ++++ 30-49 440 ++ ++ + 442 ++++ ++++ ++ 444 ++++ ++++ +++ 445 ++++ +++ + + ≧50 555 ≧50 557 ≧50 558 30-49 562 30-49 564 30-49 566 30-49 567 ≧50 572 ≧50 573 30-49 578 30-49 662 ≧50 379  1-29 375  1-29 559 ≧50 561  1-29 563  1-29 568  1-29 569  1-29 571  1-29 574  1-29 575  1-29 576  1-29 577 30-49 433  1-29 551 30-49 553  1-29 710 + 711 + 712 ++ 713 ++ 714 +++ 715 +++ 716 +

Example 11 P21 ELISA Assay

The assay was performed according to the following general protocol:

Cell Plating:

-   -   Trypsinize, count and seed SJSA1 cells at the density of 7500         cells/100 μl/well in 96-well plates a day prior to assay.     -   On the day of study, replace media with fresh RPMI-11% FBS         (assay media). Add 90 μL of the assay media per well. Control         wells with no cells, receive 100 μl media.

Peptide Dilution:

-   -   Prepare 10 mM stocks of the peptides in DMSO. Serially dilute         the stock using 1:3 dilution scheme to get 10, 3.3, 1.1, 0.33,         0.11, 0.03, 0.01 mM solutions using DMSO as diluents. Dilute the         serially DMSO-diluted peptides 33.3 times using sterile water.         This gives range of 10× working stocks. Also prepare         DMSO/sterile water (3% DMSO) mix for control wells.     -   Thus the working stocks concentration range μM will be 300, 100,         30, 10, 3, 1, 0.3 and 0 μM. Mix well at each dilution step using         multichannel.     -   Row H has controls. H1-H3 will receive 10 ul of assay media.         H4-H9 will receive 10 ul of 3% DMSO-water vehicle. H10-H12 will         have media alone control with no cells.     -   Positive control: MDM2 small molecule inhibitor, Nutlin-3a (10         mM) is used as positive control. Nutlin was diluted using the         same dilution scheme as peptides.

Addition of working stocks to cells:

-   -   Add 10 μl of 10× desired concentration to appropriate well to         achieve the final concentrations in total 100 μl volume in well.         (10 μl of 300 μM peptide+90 μl of cells in media=30 μM final         concentration in 100 μl volume in wells). Thus final         concentration range used will be 30, 10, 3, 1, 0.3& 0 μM.     -   Controls will include wells that get no peptides but contain the         same concentration of DMSO as the wells containing the peptides,         and wells containing NO CELLS.     -   20 h-post incubation, aspirate the media; wash cells with 1×PBS         (without Ca⁺⁺/Mg⁺⁺) and lyse in 60 μl of 1× Cell lysis buffer         (Cell Signaling technologies 10× buffer diluted to 1× and         supplemented with protease inhibitors and Phosphatasc         inhibitors) on ice for 30 min.     -   Centrifuge plates in at 5000 rpm speed in at 4° C. for 8 min;         collect clear supernatants and freeze at −80° C. till further         use.

Protein Estimation:

-   -   Total protein content of the lysates is measured using BCA         protein detection kit and BSA standards from Thermofisher.         Typically about 6-7 μg protein is expected per well.     -   Use 50 μl of the lysate per well to set up p21 ELISA.

Human Total p21 ELISA:

The ELISA assay protocol is followed as per the manufacturer's instructions. 50 μl lysate is used for each well, and each well is set up in triplicate.

Reagents:

-   -   Cell-Based Assay (−)-Nutlin-3 (10 mM): Cayman Chemicals, catalog         #600034     -   OptiMEM, Invitrogen catalog #51985     -   Cell Signaling Lysis Buffer (10×), Cell signaling technology,         Catalog #9803     -   Protease inhibitor Cocktail tablets(mini), Roche Chemicals,         catalog #04693124001     -   Phosphatase inhibitor Cocktail tablet, Roche Chemicals, catalog         #04906837001     -   Human total p21 ELISA kit, R&D Systems, DYC1047-5     -   STOP Solution (1M HCL), Cell Signaling Technologies, Catalog         #7002

Instruments: Micro centrifuge-Eppendorf 5415D and Multiplate Reader for Absorbance readout (Synergy 2).

Example 12 Caspase 3 Detection Assay

The assay was performed according to the following general protocol:

Cell Plating:

Trypsinize, count and seed SJSA1 cells at the density of 7500 cells/100 μl/well in 96-well plates a day prior to assay. On the day of study, replace media with fresh RPM1-11% FBS (assay media). Add 180 μL of the assay media per well. Control wells with no cells, receive 200 μl media.

Peptide dilution:

-   -   Prepare 10 mM stocks of the peptides in DMSO. Serially dilute         the stock using 1:3 dilution scheme to get 10, 3.3, 1.1, 0.33,         0.11, 0.03, 0.01 mM solutions using DMSO as diluents. Dilute the         serially DMSO-diluted peptides 33.3 times using sterile water         This gives range of 10× working stocks. Also prepare         DMSO/sterile water (3% DMSO) mix for control wells.     -   Thus the working stocks concentration range μM will be 300, 100,         30, 10, 3, 1, 0.3 and 0 μM. Mix well at each dilution step using         multichannel Add 20 ul of 10× working stocks to appropriate         wells.     -   Row H has controls. H1-H3 will receive 20 ul of assay media.         H4-H9 will receive 20 ul of 3% DMSO-water vehicle. H10-H12 will         have media alone control with no cells.     -   Positive control: MDM2 small molecule inhibitor, Nutlin-3a (10         mM) is used as positive control. Nutlin was diluted using the         same dilution scheme as peptides.

Addition of working stocks to cells:

-   -   Add 10 μl of 10× desired concentration to appropriate well to         achieve the final concentrations in total 100 μl volume in well.         (10 μl of 300 μM peptide+90 μl of cells in media=30 μM final         concentration in 100 μl volume in wells). Thus final         concentration range used will be 30, 10, 3, 1, 0.3& 0 μM.     -   Controls will include wells that get no peptides but contain the         same concentration of DMSO as the wells containing the peptides,         and wells containing NO CELLS.     -   48 h-post incubation, aspirate 80 μl media from each well; add         100 μl Caspase3/7Glo assay reagent (Promega Caspase 3/7 glo         assay system, G8092) per well, incubate with gentle shaking for         1 h at room temperature.     -   read on Synergy Biotek multiplate reader for luminescence.     -   Data is analyzed as Caspase 3 activation over DMSO-treated         cells.

Results from Examples 11 and 12 are shown in Table 7:

TABLE 7 caspase caspase caspase caspase caspase p21 p21 p21 p21 p21 SP# 0.3 uM 1 uM 3 uM 10 uM 30 uM 0.3 uM 1 uM 3 uM 10 uM 30 uM 4 9 37 35 317 3049 3257 7 0.93 1.4 5.08 21.7 23.96 18 368 1687 2306 8 1 19 25 34 972 2857 10 1 1 17 32 10 89 970 2250 11 1 5 23 33.5 140 350 2075.5 3154 26 1 1 3 14 50 8 29 29 44 646 1923 1818 65 1 6 28 34 −69 −24 122 843 1472 69 4.34 9.51 16.39 26.59 26.11 272 458.72 1281.39 2138.88 1447.22 70 1 9 26 −19 68 828 1871 71 0.95 1.02 3.68 14.72 23.52 95 101 1204 2075 72 1 1 4 10 −19 57 282 772 1045 77 1 2 19 23 80 1 2 13 20 81 1 1 6 21 0 0 417 1649 99 1 7 31 33 −19 117 370 996 1398 109 4 16 25 161 445 1221 1680 114 1 6 28 34 −21 11 116 742 910 115 1 10 26 32 −10 36 315 832 1020 118 1 2 18 27 −76 −62 −11 581 1270 120 2 11 20 30 −4 30 164 756 1349 121 1 5 19 30 9 33 81 626 1251 122 1 2 15 30 −39 −18 59 554 1289 123 1 1 6 14 125 1 3 9 29 50 104 196 353 1222 126 1 1 6 30 −47 −10 90 397 1443 127 1 1 4 13 130 1 2 6 17 139 1 2 9 18 142 1 2 15 20 144 1 4 10 16 148 1 11 23 31 −23 55 295 666 820 149 1 2 4 10 35 331 601 1164 1540 150 2 11 19 35 −37 24 294 895 906 153 2 10 15 20 154 2.68 4 13.93 19.86 30.14 414.04 837.45 1622.42 2149.51 2156.98 158 1 1.67 5 16.33 −1.5 95 209.5 654 1665.5 160 2 10 16 31 −43 46 373 814 1334 161 2 8 14 22 13 128 331 619 1078 170 1 1 16 20 175 1 5 12 21 −65 1 149 543 1107 177 1 1 8 20 183 1 1 4 8 −132 −119 −14 1002 818 196 1 4 33 26 −49 −1 214 1715 687 197 1 1 10 20 203 1 3 12 10 77 329 534 1805 380 204 1 4 10 10 3 337 928 1435 269 218 1 2 8 18 219 1 5 17 34 28 53 289 884 1435 221 1 3 6 12 127 339 923 1694 1701 223 1 1 5 18 230 1 2 3 11 245.5 392 882 1549 2086 233 6 8 17 22 23 2000 2489 3528 3689 2481 237 1 5 9 15 0 0 2 284 421 238 1 2 4 21 0 149 128 825 2066 242 1 4 5 18 0 0 35 577 595 243 1 2 5 23 0 0 0 456 615 244 1 2 7 17 0 178 190 708 1112 245 1 3 9 16 0 0 0 368 536 247 1 3 11 24 0 0 49 492 699 248 0 50 22 174 1919 249 2 5 11 23 0 0 100 907 1076 251 0 0 0 0 0 252 0 0 0 0 0 253 0 0 0 0 0 254 1 3 7 14 22 118 896 1774 3042 3035 286 1 4 11 20 22 481 1351 2882 3383 2479 287 1 1 3 11 23 97 398 986 2828 3410 315 11 14.5 25.5 32 34 2110 2209 2626 2965 2635 316 6.5 10.5 21 32 32.5 1319 1718 2848 2918 2540 317 3 4 9 26 35 551 624 776 1367 1076 331 4.5 8 11 14.5 30.5 1510 1649 2027 2319 2509 338 1 5 23 20 29 660.37 1625.38 3365.87 2897.62 2727 341 3 8 11 14 21 1325.62 1873 2039.75 2360.75 2574 343 1 1 2 5 29 262 281 450 570 1199 346 235.86 339.82 620.36 829.32 1695.78 347 2 3 5 8 29 374 622 659 905 1567 349 1 8 11 16 24 1039.5 1598.88 1983.75 2191.25 2576.38 351 3 9 13 15 24 1350.67 1710.67 2030.92 2190.67 2668.54 353 1 2 5 7 30 390 490 709 931 1483 355 1 4 11 13 30 191 688 1122 1223 1519 357 2 7 11 15 23 539 777 1080 1362 1177 358 1 2 3 6 24 252 321 434 609 1192 359 3 9 11 13 23 1163.29 1508.79 1780.29 2067.67 2479.29 416 33.74 39.82 56.57 86.78 1275.28 417 0 0 101.13 639.04 2016.58 419 58.28 97.36 221.65 1520.69 2187.94 432 54.86 68.86 105.11 440.28 1594.4

Example 13 Cell Lysis by Peptidomimetic Macrocycles

SJSA-1 cells were plated out one day in advance in clear flat-bottom plates (Costar, catalog number 353072) at 7500 cells/well with 100 ul/well of growth media, leaving row H columns 10-12 empty for media alone. On the day of the assay, media was exchanged with RPMI 1% FBS media, 90 uL of media per well.

10 mM stock solutions of the peptidomimetic macrocycles were prepared in 100% DMSO. Peptidomimetic macrocycles were then diluted serially in 100% DMSO, and then further diluted 20-fold in sterile water to prepare working stock solutions in 5% DMSO/water of each peptidomimetic macrocycle at concentrations ranging from 500 uM to 62.5 uM.

10 uL of each compound was added to the 90 uL of SJSA-1 cells to yield final concentrations of 50 uM to 6.25 uM in 0.5% DMSO-containing media. The negative control (non-lytic) sample was 0.5% DMSO alone and positive control (lytic) samples include 10 uM Melittin and 1% Triton X-100.

Cell plates were incubated for 1 hour at 37C. After the 1 hour incubation, the morphology of the cells is examined by microscope and then the plates were centrifuged at 1200 rpm for 5 minutes at room temperature. 40 uL of supernatant for each peptidomimetic macrocycle and control sample is transferred to clear assay plates. LDH release is measured using the LDH cytotoxicity assay kit from Caymen, catalog #1000882.

Results are shown in Table 8:

TABLE 8 6.25 uM % 12.5 uM % 25 uM % 50 uM % Lysed cells Lysed cells Lysed cells Lysed cells SP# (1 h LDH) (1 h LDH) (1 h LDH) (1 h LDH) 3 1 0 1 3 4 −2 1 1 2 6 1 1 1 1 7 0 0 0 0 8 −1 0 1 1 9 −3 0 0 2 11 −2 1 2 3 15 1 2 2 5 18 0 1 2 4 19 2 2 3 21 22 0 −1 0 0 26 2 5 −1 0 32 0 0 2 0 39 0 −1 0 3 43 0 0 −1 −1 55 1 5 9 13 65 0 0 0 2 69 1 0.5 −0.5 5 71 0 0 0 0 72 2 1 0 3 75 −1 3 1 1 77 −2 −2 1 −1 80 0 1 1 5 81 1 1 0 0 82 0 0 0 1 99 1.5 3 2 3.5 108 0 0 0 1 114 3 −1 4 9 115 0 1 −1 6 118 4 2 2 4 120 0 −1 0 6 121 1 0 1 7 122 1 3 0 6 123 −2 2 5 3 125 0 1 0 2 126 1 2 1 1 130 1 3 0 −1 139 −2 −3 −1 −1 142 1 0 1 3 144 1 2 −1 2 147 8 9 16 55 148 0 1 −1 0 149 6 7 7 21 150 −1 −2 0 2 153 4 3 2 3 154 −1 −1.5 −1 −1 158 0 −6 −2 160 −1 0 −1 1 161 1 1 −1 0 169 2 3 3 7 170 2 2 1 −1 174 5 3 2 5 175 3 2 1 0 177 −1 −1 0 1 182 0 2 3 6 183 2 1 0 3 190 −1 −1 0 1 196 0 −2 0 3 197 1 −4 −1 −2 203 0 −1 2 2 204 4 3 2 0 211 5 4 3 1 217 2 1 1 2 218 0 −3 −4 1 219 0 0 −1 2 221 3 3 3 11 223 −2 −2 −4 −1 230 0.5 −0.5 0 3 232 6 6 5 5 233 2.5 4.5 3.5 6 237 0 3 7 55 243 4 23 39 64 244 0 1 0 4 245 1 14 11 56 247 0 0 0 4 249 0 0 0 0 254 11 34 60 75 279 6 4 5 6 280 5 4 6 18 284 5 4 5 6 286 0 0 0 0 287 0 6 11 56 316 0 1 0 1 317 0 1 0 0 331 0 0 0 0 335 0 0 0 1 336 0 0 0 0 338 0 0 0 1 340 0 2 0 0 341 0 0 0 0 343 0 1 0 0 347 0 0 0 0 349 0 0 0 0 351 0 0 0 0 353 0 0 0 0 355 0 0 0 0 357 0 0 0 0 359 0 0 0 0 413 5 3 3 3 414 3 3 2 2 415 4 4 2 2

Example 14 p53 GRIP Assay

Thermo Scientific* Biolmage p53-MDM2 Redistribution Assay monitors the protein interaction with MDM2 and cellular translocation of GFP-tagged p53 in response to drug compounds or other stimuli. Recombinant CHO-hIR cells stably express human p53(1-312) fused to the C-terminus of enhanced green fluorescent protein (EGFP) and PDE4A4-MDM2(1-124), a fusion protein between PDE4A4 and MDM2(1-124). They provide a ready-to-use assay system for measuring the effects of experimental conditions on the interaction of p53 and MDM2. Imaging and analysis is performed with a HCS platform.

CHO-h1R cells are regularly maintained in Ham's F12 media supplemented with 1% Penicillin-Streptomycin, 0.5 mg/ml Geneticin, 1 mg/ml Zeocin and 10% FBS. Cells seeded into 96-well plates at the density of 7000 cells/100 μl per well 18-24 hours prior to running the assay using culture media. The next day, media is refreshed and PD177 is added to cells to the final concentration of 3 μM to activate foci formation. Control wells are kept without PD-177 solution. 24 h post stimulation with PD177, cells are washed once with Opti-MEM Media and 50 μL of the Opti-MEM Media supplemented with PD-177(6 μM) is added to cells. Peptides are diluted from 10 mM DMSO stocks to 500 μM working stocks in sterile water, further dilutions made in 0.5% DMSO to keep the concentration of DMSO constant across the samples. Final highest DMSO concentration is 0.5% and is used as the negative control. Cayman Chemicals Cell-Based Assay (−)-Nutlin-3 (10 mM) is used as positive control. Nutlin was diluted using the same dilution scheme as peptides. 50 μl of 2× desired concentrations is added to the appropriate well to achieve the final desired concentrations. Cells are then incubated with peptides for 6 h at 37° C. in humidified 5% CO2 atmosphere. Post-incubation period, cells are fixed by gently aspirating out the media and adding 150 μl of fixing solution per well for 20 minutes at room temperature. Fixed cells are washed 4 times with 200 μl PBS per well each time. At the end of last wash, 100 μl of 1 μM Hoechst staining solution is added. Sealed plates incubated for at least 30 min in dark, washed with PBS to remove excess stain and PBS is added to each well. Plates can be stored at 4° C. in dark up to 3 days. The translocation of p53/MDM2 is imaged using Molecular translocation module on Cellomics Arrayscan instrument using 10× objective, XF-100 filter sets for Hoechst and GFP. The output parameters was Mean-CircRINGAveIntenRatio (the ratio of average fluorescence intensities of nucleus and cytoplasm, (well average)). The minimally acceptable number of cells per well used for image analysis was set to 500 cells.

Example 15 MCF-7 Breast Cancer Study Using SP315, SP249 and SP154

A xenograft study was performed to test the efficacy of SP315, SP249 and SP154 in inhibiting tumor growth in athymic mice in the MCF-7 breast cancer xenograft model. A negative control stapled peptide. SP252, a point mutation of SP154 (F to A at position 19) was also tested in one group; this peptide had shown no activity in the SJSA-1 in vitro viability assay. Slow release 90 day 0.72 mg 17β-estradiol pellets (Innovative Research, Sarasota, Fla.) were implanted subcutaneously (sc) on the nape of the neck one day prior to tumor cell implantation (Day −1). On Day 0, MCF-7 tumor cells were implanted sc in the flank of female nude (Crl:NU-Foxnlnu) mice. On Day 18, the resultant sc tumors were measured using calipers to determine their length and width and the mice were weighed. The tumor sizes were calculated using the formula (length×width²)/2 and expressed as cubic millimeters (mm³). Mice with tumors smaller than 85.3 mm³ or larger than 417.4 mm³ were excluded from the subsequent group formation. Thirteen groups of mice, 10 mice per group, were formed by randomization such that the group mean tumor sizes were essentially equivalent (mean of groups±standard deviation of groups=180.7±17.5 mm³)

SP315, SP249, SP154 and SP252 dosing solutions were prepared from peptides formulated in a vehicle containing MPEG(2K)-DSPE at 50 mg/mL concentration in a 10 mM Histidine buffered saline at pH 7. This formulation was prepared once for the duration of the study. This vehicle was used as the vehicle control in the subsequent study.

Each group was assigned to a different treatment regimen. Group 1, as the vehicle negative control group, received the vehicle administered at 8 mL/kg body weight intravenously(iv) three times per week from Days 18-39. Groups 2 and 3 received SP154 as an iv injection at 30 mg/kg three times per week or 40 mg/kg twice a week, respectively. Group 4 received 6.7 mg/kg SP249 as an iv injection three times per week. Groups 5, 6, 7 and 8 received SP315 as an iv injection of 26.7 mg/kg three times per week, 20 mg/kg twice per week, 30 mg/kg twice per week, or 40 mg/kg twice per week, respectively. Group 9 received 30 mg/kg SP252 as an iv injection three times per week.

During the dosing period the mice were weighed and tumors measured 1-2 times per week. Results in terms of tumor volume are shown in FIGS. 3-6 and tumor growth inhibition compared with the vehicle group, body weight change and number of mice with ≧20% body weight loss or death are shown in Table 9. Tumor growth inhibition (TGT) was calculated as % TGI=100−[(TuVol^(Treated-day x)−TuVol^(Treated-day18))/(TuVol^(Vehicle negative control-day x)−TuVol^(Vehicle negative control-day 18))*100, where x=day that effect of treatment is being assessed. Group 1, the vehicle negative control group, showed good tumor growth rate for this tumor model.

For SP154, in the group dosed with 40 mg/kg twice a week 2 mice died during treatment, indicating that this dosing regimen was not tolerable. The dosing regimen of 30 mg/kg of SP154 three times per week was well-tolerated and yielded a TGI of 84%.

For SP249, the group dosed with 6.7 mg/kg three times per week 4 mice died during treatment, indicating that this dosing regimen was not tolerable.

All dosing regimens used for SP315 showed good tolerability, with no body weight loss or deaths noted. Dosing with 40 mg/kg of SP315 twice per week produced the highest TGI (92%). The dosing regimens of SP315 of 26.7 mg/kg three times per week, 20 mg/kg twice per week, 30 mg/kg twice per week produced TGI of 86, 82, and 85%, respectively.

For SP252, the point mutation of SP154 which shows no appreciable activity in in vitro assays, dosing with 30 mg/kg three times per week was well-tolerated with no body weight loss or deaths noted. While TGI of 88% was noted by Day 32, that TGI was reduced to 41% by Day 39.

Results from this Example are shown in FIGS. 3-6 and are summarized in Table 9.

TABLE 9 No. with ≧20% Group % BW No. with ≧10% BW Loss or Number Treatment Group Change BW Loss death % TGI 1 Vehicle +8.6 0/10 0/10 — 2 SP154 30 mg/kg 3×/wk iv +5.7 0/10 0/10 *84 3 SP154 40 mg/kg v 2×/wk iv N/A 0/10 2/10 Regimen (2 deaths) not tolerated 4 SP249 6.7 mg/kg 3×/wk iv N/A 6/10 4/10 Regimen not tolerated 5 SP315 26.7 mg/kg 3×/wk iv +3.7 0/10 0/10 *86 6 SP315 20 mg/kg 2×/wk iv +3.9 0/10 0/10 *82 7 SP315 30 mg/kg 2×/wk iv +8.0 0/10 0/10 *85 8 SP315 40 mg/kg 2×/wk iv +2.1 0/10 0/10 *92 9 SP252 30 mg/kg 3×/wk iv +3.3 0/10 0/10 *41 *p ≦ 0.05 Vs Vehicle Control

Example 21 Solubility Determination for Peptidomimetic Macrocycles

Peptidomimetic macrocycles are first dissolved in neat N,N-dimethylacetamide (DMA, Sigma-Aldrich, 38840-1L-F) to make 20× stock solutions over a concentration range of 20-140 mg/mL. The DMA stock solutions are diluted 20-fold in an aqueous vehicle containing 2% Solutol-HS-15, 25 mM Histidine, 45 mg/mL Mannitol to obtain final concentrations of 1-7 mg/ml of the peptidomimetic macrocycles in 5% DMA, 2% Solutol-HS-15, 25 mM Histidine, 45 mg/mL Mannitol. The final solutions are mixed gently by repeat pipetting or light vortexing, and then the final solutions are sonicated for 10 min at room temperature in an ultrasonic water bath. Careful visual observation is then performed under hood light using a 7× visual amplifier to determine if precipitate exists on the bottom or as a suspension. Additional concentration ranges are tested as needed to determine the maximum solubility limit for each peptidomimetic macrocycle.

Results from this Example are shown in FIG. 7.

Example 22 Preparation of Peptidomimetic Macrocycles Using a Boc-Protected Amino Acid

Peptidomimetic macrocycle precursors were prepared as described in Example 2 comprising an R8 amino acid at position “i” and an S5 amino acid at position “i+7”. The amino acid at position “i+3” was a Boc-protected tryptophan which was incorporated during solid-phase synthesis. Specifically, the Boc-protected tryptophan amino acid shown below (and commercially available, for example, from Novabiochem) was using during solid phase synthesis:

Metathesis was performed using a ruthenium catalyst prior to the cleavage and deprotection steps. The composition obtained following cyclization was determined by HPLC analysis to contain primarily peptidomimetic macrocycles having a crosslinker comprising a trans olefin (“iso2”, comprising the double bond in an E configuration). Unexpectedly, a ratio of 90:10 was observed for the trans and cis products, respectively. 

What is claimed is:
 1. A peptidomimetic macrocycle of Formula:

or a pharmaceutically-acceptable salt thereof wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is independently an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), where each of X₄ and X₁₁ is independently an amino acid; each D is independently an amino acid; each E is independently an amino acid selected from the group consisting of Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine); R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L and L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-; each L₁ and L₂ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄-]_(n), each being optionally substituted with R₅; each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; R₅ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; v is an integer from 1-1000; w is an integer from 3-1000; and n is an integer from 1-5.
 2. A peptidomimetic macrocycle comprising an amino acid sequence which is at least about 60% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c, wherein the peptidomimetic macrocycle has the formula:

or a pharmaceutically-acceptable salt thereof, wherein: each A, C, and D is independently an amino acid; each B is independently an amino acid,

[—NH-L₃-CO—], [—NH-L₃-SO₂—], or [—NH-L₃-]; each E is independently an amino acid selected from the group consisting of Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine); each R₁ and R₂ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each L and L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-; each L₁ and L₂ and L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅; each R₄ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v is independently an integer from 1-1000; each w is independently an integer from 3-1000; u is an integer from 1-10; each x, y and z is independently an integer from 0-10; and each n is independently an integer from 1-5.
 3. A peptidomimetic macrocycle of Formula:

or pharmaceutically-acceptable salt thereof wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xa₁₀ is independently an amino acid, wherein at least three of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acids as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂ (SEQ ID NO: 8) or Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), wherein each X₄ and X₁₁ is independently an amino acid; each D is independently an amino acid; each E is independently an amino acid selected from the group consisting of Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine); R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-; or forms a macrocycle-forming linker L′ connected to the alpha position of one of said D or E amino acids; each L or L′ is independently a macrocycle-forming linker; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SO₂R₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; R₇ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; R₈ is —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; v is an integer from 1-1000; and w is an integer from 3-1000.
 4. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved binding affinity to MDM2 or MDMX relative to a corresponding peptidomimetic macrocycle_(s) wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 5. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomirnetic macrocycle or pharmaceutically-acceptable salt thereof has a reduced ratio of binding affinities to MDMX versus MDM2 relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 6. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved in vitro anti-tumor efficacy against a p53 positive tumor cell line relative to a corresponding peptidomimetic macrocycle₁ wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 7. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved in vitro induction of apoptosis in a p53 positive tumor cell line relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 8. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved in vitro anti-tumor efficacy ratio for a p53 positive versus a p53 negative or a p53 mutant tumor cell line relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 9. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved in vivo anti-tumor efficacy against a p53 positive tumor relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 10. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved in vivo induction of apoptosis in a p53 positive tumor relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 11. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved cell permeability relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the corresponding peptidomimetic macrocycle.
 12. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved solubility relative to a corresponding peptidomimetic macrocycle, wherein w is 0, 1 or 2 in the correspondingpeptidomimetic macrocycle.
 13. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1 or 3, wherein Xaa₅ is Glu.
 14. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 13, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof has an improved property relative to a corresponding peptidomimetic macrocycle, wherein the improved property is selected from the group consisting of improved binding affinity, improved solubility, improved cellular efficacy, improved helicity, improved cell permeability, improved in vivo or in vitro anti-tumor efficacy, and improved induction of apoptosis, wherein Xaa₅ is Ala in the corresponding peptidomimetic macrocycle.
 15. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein [D]_(v) is -Leu₁Thr₂.
 16. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein w is 3-10.
 17. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 16, wherein w is 3-6.
 18. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 16, wherein w is 6-10.
 19. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 16, wherein w is
 6. 20. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1 or 3, wherein v is 1-10.
 21. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 20, wherein v is 2-10.
 22. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 20, wherein v is 2-5.
 23. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 20, wherein v is
 2. 24. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein [D]_(v) is -Leu₁-Thr₂.
 25. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein each L₁ and L₂ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, or heterocycloarylene, each being optionally substituted with R₅.
 26. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein each L₁ and L₂ is are independently alkylene or alkenylene.
 27. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein L is alkylene, alkenylene, or alkynylene.
 28. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 2, 27, and 3 wherein L is alkenylene.
 29. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 28, wherein L is C₃-C₁₆ alkenylene.
 30. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 29, wherein L is C₁₀-C₁₄ alkenylene.
 31. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein R₁ and R₂ are independently —H, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halo-.
 32. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein R₁ and R₂ are H.
 33. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 1, wherein R₁ and R₂ are independently alkyl.
 34. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 33, wherein R₁ and R₂ are methyl.
 35. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein x+y+z=6.
 36. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein u is
 1. 37. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2, and 3, wherein each E is independently Ser or Ala.
 38. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 39. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 40. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 41. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 42. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 43. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 44. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 45. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 46. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 47. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 48. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 49. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 50. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 51. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 52. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 53. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 54. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 55. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 56. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 57. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 58. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 59. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 60. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 61. The peptidomimetic macrocycle of claim 1, having formula:

or a pharmaceutically acceptable salt thereof.
 62. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 16, wherein w is
 3. 63. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein v is 1-10.
 64. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein v is 3-10.
 65. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein v is 3-5.
 66. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein v is
 3. 67. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 2, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof comprises an amino acid sequence which is at least about 80% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c.
 68. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 67, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof comprises an amino acid sequence which is at least about 90% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c.
 69. The peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of claim 68, wherein the peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof comprises an amino acid sequence which is at least about 95% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c.
 70. A method of treating cancer in a subject comprising administering to the subject a therapeutically-effective amount of a peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2 and
 3. 71. The method of claim 70, wherein the cancer is selected from the group consisting of head and neck cancer, melanoma, lung cancer, breast cancer, and glioma.
 72. A method of modulating the activity of p53 and/or MDM2 and/or MDMX in a subject comprising administering to the subject a therapeutically-effective amount of a peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2 and
 3. 73. A method of antagonizing the interaction between p53 and MDM2 proteins and/or between p53 and MDMX proteins in a subject comprising administering to the subject a therapeutically-effective amount of a peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of any one of claims 1, 2 and
 3. 74. A method of preparing a composition comprising a peptidomimetic macrocycle or pharmaceutically-acceptable salt thereof of Formula (Ia):

or pharmaceutically-acceptable salt thereof, comprising an amino acid sequence which is about 60% to about 100% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c, the method comprising treating a compound of Formula (II) or pharmaceutically-acceptable salt thereof

with a catalyst to result in the compound of Formula (Ia) or pharmaceutically-acceptable salt thereof, wherein in the compound of Formula (Ia) or pharmaceutically-acceptable salt thereof and in the compound of Formula (II) or pharmaceutically-acceptable salt thereof each A, C, and D is independently an amino acid;

each B is independently an amino acid [—NH-L₃-SO₂—], or [—NH-L₃-]; each E is independently an amino acid selected from the group consisting of Ala (alanine), D-Ala (D-alanine), Aib (α-aminoisobutyric acid), Sar (N-methyl glycine), and Ser (serine); each R₁ and R₂ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroalkyl, or heterocycloalkyl, unsubstituted or substituted with halogen; or forms a macrocycle-forming linker L′ connected to the alpha position of one of the D or E amino acids; each R₃ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, cycloalkylalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅; each L′ is independently a macrocycle-forming linker of the formula -L₁-L₂-; each L₁, L₂ and L₃ is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, cycloarylene, heterocycloarylene, or [—R₄-K-R₄—]_(n), each being optionally substituted with R₅; each R₄ and R_(4′) is independently alkylene, alkenylene, alkynylene, heteroalkylene, cycloalkylene, heterocycloalkylene, arylene, or heteroarylene; each K is independently O, S, SO, SO₂, CO, CO₂, or CONR₃; each R₅ is independently halogen, alkyl, —OR₆, —N(R₆)₂, —SR₆, —SOR₆, —SO₂R₆, —CO₂R₆, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₆ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, a fluorescent moiety, a radioisotope or a therapeutic agent; each R₇ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with a D residue; each R₈ is independently hydrogen, alkyl, alkenyl, alkynyl, arylalkyl, cycloalkyl, heteroalkyl, cycloalkylalkyl, heterocycloalkyl, cycloaryl, or heterocycloaryl, optionally substituted with R₅, or part of a cyclic structure with an E residue; each v is independently an integer from 1-1000; each w is independently an integer from 3-1000; u is an integer from 1-10; each x, y and z is independently an integer from 0-10; each n is independently an integer from 1-5; each o is independently an integer from 1 to 15; each p is independently an integer from 1 to 15; (E) indicates a trans double bond or an E-double bond; and one or more of A, B, and C, has a side chain bearing a protecting group.
 75. The method of claim 74, wherein the protecting group is a nitrogen atom protecting group.
 76. The method of claim 74, wherein the protecting group is a Boc group.
 77. The method of claim 75, wherein the side chain bearing the protecting group comprises a protected indole.
 78. The method of claim 77, wherein the protecting group is borne on the side chain of a tryptophan (W).
 79. The method of claim 78, wherein the protecting group is a Boc group.
 80. The method of claim 74, wherein after the step of treating the compound of Formula (II) or pharmaceutically-acceptable salt thereof with the catalyst, the compound of Formula (Ia) or pharmaceutically-acceptable salt thereof is obtained in an amount equal or higher than an amount obtained of a corresponding compound which is a Z isomer.
 81. The method of claim 80, wherein after the step of treating the compound of Formula (II) or pharmaceutically-acceptable salt thereof with the catalyst, the compound of Formula (Ia) or pharmaceutically-acceptable salt thereof is obtained in an amount that is 2, 3, 4, 5, 6, 7, 8, 9, or 10-fold higher than an amount obtained of the corresponding compound which is the Z isomer.
 82. The method of claim 74, wherein the catalyst is a ruthenium catalyst.
 83. The method of claim 74, further comprising the step of treating the compound of Formula (Ia) or pharmaceutically-acceptable salt thereof with a reducing agent or an oxidizing agent.
 84. The method of claim 74, wherein the compound of Formula (II) or parmaceutically-acceptable salt thereof is further attached to a solid support.
 85. The method of claim 74, wherein the compound of Formula (II) or pharmaceutically-acceptable salt thereof is not attached to a solid support.
 86. The method of claim 74, further comprising removing the protecting group from the compound of Formula (Ia) or pharmaceutically-acceptable salt thereof.
 87. The method of claim 74, wherein the treating is conducted at a temperature ranging from about 20° C. to about 80° C.
 88. The method of claim 74, wherein the peptidomimetic macrocycle of Formula (Ia) has the Formula:

or pharmaceutically-acceptable salt thereof, wherein: each of Xaa₃, Xaa₅, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaa₁₀ is independently an amino acid, wherein at least two of Xaa₃, Xaa₅, Xaa₆, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-His₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀-X₁₁-Ser₁₂(SEQ ID NO: 8), wherein each of X₄ and X₁₁ is independently an amino acid; v is an integer from 1-500; Xaa₇ is Boc-protected tryptophan.
 89. The method of claim 74, wherein the peptidomimetic macrocycle of Formula (Ia) has the Formula:

or pharmaceutically-acceptable salt thereof, wherein: each of Xaa₃, Xaa₈, Xaa₆, Xaa₇, Xaa₈, Xaa₉, and Xaar₁₀ is independently an amino acid, wherein at least two of Xaa₃, Xaa₅, Xaa₆, Xaa₈, Xaa₉, and Xaa₁₀ are the same amino acid as the amino acid at the corresponding position of the sequence Phe₃-X₄-Glu₅-Tyr₆-Trp₇-Ala₈-Gln₉-Leu₁₀/Cba₁₀-X₁₁-Ala₁₂ (SEQ ID NO: 9), wherein each of X₄ and X₁₁ is independently an amino acid; comprises double bond in the E configuration; v is an integer from 1-500; and Xaa₇ is Boc-protected tryptophan.
 90. The method of claim 74, wherein the peptidomimetic macrocycle of Formula (Ia) or pharmaceutically-acceptable salt thereof comprises an α-helix.
 91. The method of claim 77 or 78, wherein L is C₃-C₁₆ alkenylene.
 92. The method of claim 91, wherein L is C₁₀-C₁₄ alkenylene.
 93. The method of claim 74, wherein w is 3-10.
 94. The method of claim 74, wherein w is 3-6.
 95. The method of claim 74, wherein w is
 3. 96. The method of claim 74, wherein v is 1-10.
 97. The method of claim 74, wherein v is 3-10.
 98. The method of claim 74, wherein v is 3-5.
 99. The method of claim 74, wherein v is
 3. 100. The method of claim 74, wherein x+y+z=6 in the peptidomimetic macrocycle of Formula (Ia) or pharmaceutically-acceptable salt thereof.
 101. The method of claim 74, wherein u is
 1. 102. The method of claim 74, wherein each E is independently an amino acid selected from the group consisting of Ser and Ala.
 103. The method of claim 74, wherein the peptidomimetic macrocycle of Formula (Ia) or pharmaceutically-acceptable salt thereof comprises an amino acid sequence which is about 80% to about 100% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c.
 104. The method of claim 103, wherein the peptidomimetic macrocycle of Formula (Ia) or pharmaceutically-acceptable salt thereof comprises an amino acid sequence which is about 90% to about 100% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c.
 105. The method of claim 104, wherein the peptidomimetic macrocycle of Formula (Ia) or pharmaceutically-acceptable salt thereof comprises an amino acid sequence which is about 95% to about 100% identical to an amino acid sequence in any of Table 1, Table 1a, Table 1b, and Table 1c. 